6-157405875-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405875
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405875
    reference: chr 6
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.575C>T
  hgvsp: ENSP00000412835.2:p.Thr192Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2078C>T
  hgvsp: ENSP00000356116.1:p.Thr693Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2078C>T
  hgvsp: ENSP00000055163.7:p.Thr693Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1904C>T
  hgvsp: ENSP00000275248.4:p.Thr635Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.186C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2117C>T
  hgvsp: ENSP00000344546.4:p.Thr706Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.344C>T
  hgvsp: ENSP00000313006.6:p.Thr115Met
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8766
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr706Met
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

6-157405876-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405876
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405876
    reference: chr 6
allele count: 5
allele frequency: 4.118751853438334e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.187G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1905G>A
  hgvsp: ENST00000275248.4:c.1905G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2079G>A
  hgvsp: ENST00000350026.5:c.2079G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.576G>A
  hgvsp: ENST00000414678.2:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.345G>A
  hgvsp: ENST00000319584.6:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2118G>A
  hgvsp: ENST00000346085.5:c.2118G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2079G>A
  hgvsp: ENST00000367148.1:c.2079G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1685
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41491
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3051
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr706Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

6-157405888-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405888
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405888
    reference: chr 6
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.357G>C
  hgvsp: ENST00000319584.6:c.357G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2130G>C
  hgvsp: ENST00000346085.5:c.2130G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.588G>C
  hgvsp: ENST00000414678.2:c.588G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1917G>C
  hgvsp: ENST00000275248.4:c.1917G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.199G>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2091G>C
  hgvsp: ENST00000350026.5:c.2091G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2091G>C
  hgvsp: ENST00000367148.1:c.2091G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4663
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41490
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1358
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly710Gly
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

6-157405889-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405889
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405889
    reference: chr 6
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2092G>A
  hgvsp: ENSP00000356116.1:p.Asp698Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.358G>A
  hgvsp: ENSP00000313006.6:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.200G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2131G>A
  hgvsp: ENSP00000344546.4:p.Asp711Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1918G>A
  hgvsp: ENSP00000275248.4:p.Asp640Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.589G>A
  hgvsp: ENSP00000412835.2:p.Asp197Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2092G>A
  hgvsp: ENSP00000055163.7:p.Asp698Asn
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8743
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3050
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp711Asn
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

6-157405893-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405893
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405893
    reference: chr 6
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.204A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.593A>G
  hgvsp: ENSP00000412835.2:p.Gln198Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2135A>G
  hgvsp: ENSP00000344546.4:p.Gln712Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1922A>G
  hgvsp: ENSP00000275248.4:p.Gln641Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.362A>G
  hgvsp: ENSP00000313006.6:p.Gln121Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2096A>G
  hgvsp: ENSP00000356116.1:p.Gln699Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2096A>G
  hgvsp: ENSP00000055163.7:p.Gln699Arg
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4663
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3051
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln712Arg
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: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

6-157405903-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405903
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405903
    reference: chr 6
allele count: 7
allele frequency: 5.766347595433053e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2145G>A
  hgvsp: ENST00000346085.5:c.2145G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1932G>A
  hgvsp: ENST00000275248.4:c.1932G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.214G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.372G>A
  hgvsp: ENST00000319584.6:c.372G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.603G>A
  hgvsp: ENST00000414678.2:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.4G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2106G>A
  hgvsp: ENST00000350026.5:c.2106G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2106G>A
  hgvsp: ENST00000367148.1:c.2106G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4663
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro715Pro
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

6-157405905-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405905
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405905
    reference: chr 6
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.216C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2108C>T
  hgvsp: ENSP00000055163.7:p.Ala703Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.6C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.605C>T
  hgvsp: ENSP00000412835.2:p.Ala202Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2108C>T
  hgvsp: ENSP00000356116.1:p.Ala703Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.374C>T
  hgvsp: ENSP00000313006.6:p.Ala125Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1934C>T
  hgvsp: ENSP00000275248.4:p.Ala645Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2147C>T
  hgvsp: ENSP00000344546.4:p.Ala716Val
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4663
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala716Val
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-157405906-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405906
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405906
    reference: chr 6
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.375G>A
  hgvsp: ENST00000319584.6:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2109G>A
  hgvsp: ENST00000350026.5:c.2109G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2109G>A
  hgvsp: ENST00000367148.1:c.2109G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1935G>A
  hgvsp: ENST00000275248.4:c.1935G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.606G>A
  hgvsp: ENST00000414678.2:c.606G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.7G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2148G>A
  hgvsp: ENST00000346085.5:c.2148G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.217G>A
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4663
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1685
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3039
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala716Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/6-157405907-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405907
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405907
    reference: chr 6
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.218C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.376C>A
  hgvsp: ENSP00000313006.6:p.Gln126Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2149C>A
  hgvsp: ENSP00000344546.4:p.Gln717Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2110C>A
  hgvsp: ENSP00000055163.7:p.Gln704Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1936C>A
  hgvsp: ENSP00000275248.4:p.Gln646Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.607C>A
  hgvsp: ENSP00000412835.2:p.Gln203Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.8C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2110C>A
  hgvsp: ENSP00000356116.1:p.Gln704Lys
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3045
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1984
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln717Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

6-157405909-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405909
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405909
    reference: chr 6
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2112G>C
  hgvsp: ENSP00000055163.7:p.Gln704His
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.378G>C
  hgvsp: ENSP00000313006.6:p.Gln126His
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2151G>C
  hgvsp: ENSP00000344546.4:p.Gln717His
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.609G>C
  hgvsp: ENSP00000412835.2:p.Gln203His
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2112G>C
  hgvsp: ENSP00000356116.1:p.Gln704His
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.10G>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1938G>C
  hgvsp: ENSP00000275248.4:p.Gln646His
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.220G>C
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4661
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3044
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41496
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln717His
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

6-157405911-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405911
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405911
    reference: chr 6
allele count: 4
allele frequency: 3.295055768818887e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1940C>T
  hgvsp: ENSP00000275248.4:p.Ser647Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2114C>T
  hgvsp: ENSP00000055163.7:p.Ser705Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2153C>T
  hgvsp: ENSP00000344546.4:p.Ser718Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.611C>T
  hgvsp: ENSP00000412835.2:p.Ser204Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.12C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.222C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2114C>T
  hgvsp: ENSP00000356116.1:p.Ser705Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.380C>T
  hgvsp: ENSP00000313006.6:p.Ser127Leu
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4660
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser718Leu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

6-157405912-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405912
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405912
    reference: chr 6
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2154G>A
  hgvsp: ENST00000346085.5:c.2154G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.223G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2115G>A
  hgvsp: ENST00000367148.1:c.2115G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2115G>A
  hgvsp: ENST00000350026.5:c.2115G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.612G>A
  hgvsp: ENST00000414678.2:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1941G>A
  hgvsp: ENST00000275248.4:c.1941G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.13G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.381G>A
  hgvsp: ENST00000319584.6:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1364
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser718Ser
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

6-157405926-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405926
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405926
    reference: chr 6
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2168A>G
  hgvsp: ENSP00000344546.4:p.His723Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.626A>G
  hgvsp: ENSP00000412835.2:p.His209Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2129A>G
  hgvsp: ENSP00000356116.1:p.His710Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1955A>G
  hgvsp: ENSP00000275248.4:p.His652Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.395A>G
  hgvsp: ENSP00000313006.6:p.His132Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.237A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.27A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2129A>G
  hgvsp: ENSP00000055163.7:p.His710Arg
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41508
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His723Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

6-157405927-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405927
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405927
    reference: chr 6
allele count: 11
allele frequency: 9.061552655858706e-5
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.396T>C
  hgvsp: ENST00000319584.6:c.396T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.28T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2130T>C
  hgvsp: ENST00000367148.1:c.2130T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2130T>C
  hgvsp: ENST00000350026.5:c.2130T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.627T>C
  hgvsp: ENST00000414678.2:c.627T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2169T>C
  hgvsp: ENST00000346085.5:c.2169T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.238T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1956T>C
  hgvsp: ENST00000275248.4:c.1956T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1356
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His723His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

6-157405929-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405929
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405929
    reference: chr 6
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.398C>T
  hgvsp: ENSP00000313006.6:p.Ala133Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1958C>T
  hgvsp: ENSP00000275248.4:p.Ala653Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2171C>T
  hgvsp: ENSP00000344546.4:p.Ala724Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.240C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2132C>T
  hgvsp: ENSP00000055163.7:p.Ala711Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2132C>T
  hgvsp: ENSP00000356116.1:p.Ala711Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.30C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.629C>T
  hgvsp: ENSP00000412835.2:p.Ala210Val
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4663
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41512
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala724Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

6-157405930-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405930
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405930
    reference: chr 6
allele count: 62986
allele frequency: 5.190440873506387e-1
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2133G>A
  hgvsp: ENST00000367148.1:c.2133G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.399G>A
  hgvsp: ENST00000319584.6:c.399G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.630G>A
  hgvsp: ENST00000414678.2:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2172G>A
  hgvsp: ENST00000346085.5:c.2172G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.31G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2133G>A
  hgvsp: ENST00000350026.5:c.2133G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.241G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1959G>A
  hgvsp: ENST00000275248.4:c.1959G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33424
  bin: 9.75e1
  variant carriers: 33256
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 534
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 9.25e1
  variant carriers: 2353
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 6.75e1
  variant carriers: 927
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 2.75e1
  variant carriers: 174
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 2.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 7.75e1
  variant carriers: 1464
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 3.25e1
  variant carriers: 268
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.25e1
  variant carriers: 680
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 3.75e1
  variant carriers: 283
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.25e1
  variant carriers: 408
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 4.25e1
  variant carriers: 302
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 4.75e1
  variant carriers: 342
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 8.75e1
  variant carriers: 2138
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 7.25e1
  variant carriers: 1195
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 8.25e1
  variant carriers: 1752
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 8.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 5348
  bin: 6.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala724Ala
num of homozygotes: 16778
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

6-157405941-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405941
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405941
    reference: chr 6
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1970T>G
  hgvsp: ENSP00000275248.4:p.Leu657Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.42T>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2144T>G
  hgvsp: ENSP00000356116.1:p.Leu715Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.252T>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2144T>G
  hgvsp: ENSP00000055163.7:p.Leu715Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.410T>G
  hgvsp: ENSP00000313006.6:p.Leu137Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.641T>G
  hgvsp: ENSP00000412835.2:p.Leu214Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2183T>G
  hgvsp: ENSP00000344546.4:p.Leu728Arg
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3454
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4284
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu728Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-157405945-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405945
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405945
    reference: chr 6
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2148C>T
  hgvsp: ENST00000367148.1:c.2148C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2187C>T
  hgvsp: ENST00000346085.5:c.2187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2148C>T
  hgvsp: ENST00000350026.5:c.2148C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.645C>T
  hgvsp: ENST00000414678.2:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.256C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.414C>T
  hgvsp: ENST00000319584.6:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.46C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1974C>T
  hgvsp: ENST00000275248.4:c.1974C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8788
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3453
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11708
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser729Ser
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

6-157405952-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405952
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405952
    reference: chr 6
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1981C>G
  hgvsp: ENSP00000275248.4:p.Pro661Ala
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2155C>G
  hgvsp: ENSP00000356116.1:p.Pro719Ala
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.652C>G
  hgvsp: ENSP00000412835.2:p.Pro218Ala
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.263C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.53C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2155C>G
  hgvsp: ENSP00000055163.7:p.Pro719Ala
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2194C>G
  hgvsp: ENSP00000344546.4:p.Pro732Ala
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.421C>G
  hgvsp: ENSP00000313006.6:p.Pro141Ala
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22274
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro732Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

6-157405954-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405954
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405954
    reference: chr 6
allele count: 5
allele frequency: 4.119905736556747e-5
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1983G>A
  hgvsp: ENST00000275248.4:c.1983G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.654G>A
  hgvsp: ENST00000414678.2:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.265G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2157G>A
  hgvsp: ENST00000367148.1:c.2157G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.423G>A
  hgvsp: ENST00000319584.6:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.55G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2196G>A
  hgvsp: ENST00000346085.5:c.2196G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2157G>A
  hgvsp: ENST00000350026.5:c.2157G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5324
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3446
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro732Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-157405955-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405955
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405955
    reference: chr 6
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2158G>A
  hgvsp: ENSP00000356116.1:p.Gly720Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2158G>A
  hgvsp: ENSP00000055163.7:p.Gly720Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.424G>A
  hgvsp: ENSP00000313006.6:p.Gly142Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1984G>A
  hgvsp: ENSP00000275248.4:p.Gly662Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.655G>A
  hgvsp: ENSP00000412835.2:p.Gly219Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2197G>A
  hgvsp: ENSP00000344546.4:p.Gly733Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.266G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.56G>A
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3450
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly733Arg
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-157405956-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405956
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405956
    reference: chr 6
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2159G>C
  hgvsp: ENSP00000356116.1:p.Gly720Ala
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1985G>C
  hgvsp: ENSP00000275248.4:p.Gly662Ala
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2198G>C
  hgvsp: ENSP00000344546.4:p.Gly733Ala
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.57G>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2159G>C
  hgvsp: ENSP00000055163.7:p.Gly720Ala
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.425G>C
  hgvsp: ENSP00000313006.6:p.Gly142Ala
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.267G>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.656G>C
  hgvsp: ENSP00000412835.2:p.Gly219Ala
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3447
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly733Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

6-157405959-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405959
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405959
    reference: chr 6
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2201G>A
  hgvsp: ENSP00000344546.4:p.Gly734Asp
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2162G>A
  hgvsp: ENSP00000356116.1:p.Gly721Asp
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.659G>A
  hgvsp: ENSP00000412835.2:p.Gly220Asp
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.428G>A
  hgvsp: ENSP00000313006.6:p.Gly143Asp
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1988G>A
  hgvsp: ENSP00000275248.4:p.Gly663Asp
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2162G>A
  hgvsp: ENSP00000055163.7:p.Gly721Asp
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.60G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.270G>A
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8395
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4274
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3145
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11647
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly734Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP

6-157405967-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405967
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405967
    reference: chr 6
allele count: 11
allele frequency: 9.062896501721951e-5
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.1996C>T
  hgvsp: ENSP00000275248.4:p.Pro666Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2209C>T
  hgvsp: ENSP00000344546.4:p.Pro737Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.436C>T
  hgvsp: ENSP00000313006.6:p.Pro146Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.68C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2170C>T
  hgvsp: ENSP00000055163.7:p.Pro724Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.278C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.667C>T
  hgvsp: ENSP00000412835.2:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2170C>T
  hgvsp: ENSP00000356116.1:p.Pro724Ser
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3146
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22383
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro737Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

6-157405978-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405978
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405978
    reference: chr 6
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2007T>A
  hgvsp: ENST00000275248.4:c.2007T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2181T>A
  hgvsp: ENST00000350026.5:c.2181T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.79T>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.447T>A
  hgvsp: ENST00000319584.6:c.447T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.289T>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2181T>A
  hgvsp: ENST00000367148.1:c.2181T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.678T>A
  hgvsp: ENST00000414678.2:c.678T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2220T>A
  hgvsp: ENST00000346085.5:c.2220T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3430
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4272
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8394
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val740Val
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum

6-157405981-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405981
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405981
    reference: chr 6
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.292C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.450C>T
  hgvsp: ENST00000319584.6:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.681C>T
  hgvsp: ENST00000414678.2:c.681C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2184C>T
  hgvsp: ENST00000350026.5:c.2184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2184C>T
  hgvsp: ENST00000367148.1:c.2184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2223C>T
  hgvsp: ENST00000346085.5:c.2223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2010C>T
  hgvsp: ENST00000275248.4:c.2010C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.82C>T
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly741Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS

6-157405985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405985
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405985
    reference: chr 6
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.86C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2188C>T
  hgvsp: ENSP00000356116.1:p.Pro730Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2188C>T
  hgvsp: ENSP00000055163.7:p.Pro730Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.296C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2014C>T
  hgvsp: ENSP00000275248.4:p.Pro672Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.685C>T
  hgvsp: ENSP00000412835.2:p.Pro229Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2227C>T
  hgvsp: ENSP00000344546.4:p.Pro743Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.454C>T
  hgvsp: ENSP00000313006.6:p.Pro152Ser
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22383
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro743Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD

6-157405988-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405988
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405988
    reference: chr 6
allele count: 2
allele frequency: 1.648288252649623e-5
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.89G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.688G>A
  hgvsp: ENSP00000412835.2:p.Val230Ile
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.457G>A
  hgvsp: ENSP00000313006.6:p.Val153Ile
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2230G>A
  hgvsp: ENSP00000344546.4:p.Val744Ile
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2017G>A
  hgvsp: ENSP00000275248.4:p.Val673Ile
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2191G>A
  hgvsp: ENSP00000356116.1:p.Val731Ile
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2191G>A
  hgvsp: ENSP00000055163.7:p.Val731Ile
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.299G>A
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3145
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val744Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

6-157405994-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405994
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405994
    reference: chr 6
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2236A>G
  hgvsp: ENSP00000344546.4:p.Ser746Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.305A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2197A>G
  hgvsp: ENSP00000356116.1:p.Ser733Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2023A>G
  hgvsp: ENSP00000275248.4:p.Ser675Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.694A>G
  hgvsp: ENSP00000412835.2:p.Ser232Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.463A>G
  hgvsp: ENSP00000313006.6:p.Ser155Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2197A>G
  hgvsp: ENSP00000055163.7:p.Ser733Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.95A>G
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22373
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3418
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser746Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

6-157405998-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157405998
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157405998
    reference: chr 6
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2201A>G
  hgvsp: ENSP00000356116.1:p.Asn734Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2027A>G
  hgvsp: ENSP00000275248.4:p.Asn676Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.467A>G
  hgvsp: ENSP00000313006.6:p.Asn156Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2240A>G
  hgvsp: ENSP00000344546.4:p.Asn747Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.698A>G
  hgvsp: ENSP00000412835.2:p.Asn233Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2201A>G
  hgvsp: ENSP00000055163.7:p.Asn734Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.99A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.309A>G
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2011
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4263
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asn747Ser
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-157406007-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406007
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406007
    reference: chr 6
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2210G>A
  hgvsp: ENSP00000356116.1:p.Arg737Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2249G>A
  hgvsp: ENSP00000344546.4:p.Arg750Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.476G>A
  hgvsp: ENSP00000313006.6:p.Arg159Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.108G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.707G>A
  hgvsp: ENSP00000412835.2:p.Arg236Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2036G>A
  hgvsp: ENSP00000275248.4:p.Arg679Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.318G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2210G>A
  hgvsp: ENSP00000055163.7:p.Arg737Gln
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5277
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg750Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff

6-157406025-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406025
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406025
    reference: chr 6
allele count: 1
allele frequency: 8.324869715788949e-6
allele num: 120122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2054C>T
  hgvsp: ENSP00000275248.4:p.Pro685Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.126C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.336C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2228C>T
  hgvsp: ENSP00000055163.7:p.Pro743Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.494C>T
  hgvsp: ENSP00000313006.6:p.Pro165Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.725C>T
  hgvsp: ENSP00000412835.2:p.Pro242Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2267C>T
  hgvsp: ENSP00000344546.4:p.Pro756Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2228C>T
  hgvsp: ENSP00000356116.1:p.Pro743Leu
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3305
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5191
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3134
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro756Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

6-157406027-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406027
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406027
    reference: chr 6
allele count: 1
allele frequency: 8.332083520805212e-6
allele num: 120018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2230G>A
  hgvsp: ENSP00000055163.7:p.Ala744Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.727G>A
  hgvsp: ENSP00000412835.2:p.Ala243Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.128G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.496G>A
  hgvsp: ENSP00000313006.6:p.Ala166Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2269G>A
  hgvsp: ENSP00000344546.4:p.Ala757Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2230G>A
  hgvsp: ENSP00000356116.1:p.Ala744Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.338G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2056G>A
  hgvsp: ENSP00000275248.4:p.Ala686Thr
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14873
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11592
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8081
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4213
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala757Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

6-157406029-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406029
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406029
    reference: chr 6
allele count: 1
allele frequency: 8.345852111500584e-6
allele num: 119820
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.729A>G
  hgvsp: ENST00000414678.2:c.729A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2232A>G
  hgvsp: ENST00000350026.5:c.2232A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.130A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2271A>G
  hgvsp: ENST00000346085.5:c.2271A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2058A>G
  hgvsp: ENST00000275248.4:c.2058A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.340A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.498A>G
  hgvsp: ENST00000319584.6:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2232A>G
  hgvsp: ENST00000367148.1:c.2232A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5168
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1996
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4210
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala757Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

6-157406033-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406033
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406033
    reference: chr 6
allele count: 1
allele frequency: 8.392923087252828e-6
allele num: 119148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.134A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2236A>G
  hgvsp: ENSP00000356116.1:p.Ile746Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2275A>G
  hgvsp: ENSP00000344546.4:p.Ile759Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2062A>G
  hgvsp: ENSP00000275248.4:p.Ile688Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2236A>G
  hgvsp: ENSP00000055163.7:p.Ile746Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.733A>G
  hgvsp: ENSP00000412835.2:p.Ile245Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.502A>G
  hgvsp: ENSP00000313006.6:p.Ile168Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.344A>G
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20315
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7785
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile759Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/6-157406035-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406035
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406035
    reference: chr 6
allele count: 1
allele frequency: 8.400961069946402e-6
allele num: 119034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2064C>A
  hgvsp: ENST00000275248.4:c.2064C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.136C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.346C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2277C>A
  hgvsp: ENST00000346085.5:c.2277C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.735C>A
  hgvsp: ENST00000414678.2:c.735C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2238C>A
  hgvsp: ENST00000367148.1:c.2238C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2238C>A
  hgvsp: ENST00000350026.5:c.2238C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.504C>A
  hgvsp: ENST00000319584.6:c.504C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2423
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7752
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20205
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile759Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

6-157406046-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406046
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406046
    reference: chr 6
allele count: 5
allele frequency: 4.266502832957881e-5
allele num: 117192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.140+7A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2242+7A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2242+7A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2068+7A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2281+7A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.350+7A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.739+7A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.508+7A>T
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3191
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5105
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18062
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11583
  bin: 9.75e1
  variant carriers: 5
hgvs: c.2281+7A>T
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

6-157406052-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406052
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406052
    reference: chr 6
allele count: 1
allele frequency: 8.597860852219967e-6
allele num: 116308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.739+13C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.350+13C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2242+13C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2242+13C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2068+13C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.140+13C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2281+13C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.508+13C>G
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5257
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4446
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4175
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

6-157406054-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406054
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406054
    reference: chr 6
allele count: 1
allele frequency: 8.620986930583814e-6
allele num: 115996
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2281+15G>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2242+15G>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.508+15G>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2242+15G>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.140+15G>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2068+15G>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.739+15G>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.350+15G>C
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3148
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4557
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5074
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3124
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/6-157406056-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406056
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406056
    reference: chr 6
allele count: 1
allele frequency: 8.64737725047993e-6
allele num: 115642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.350+17C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2242+17C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.140+17C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.508+17C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2068+17C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2242+17C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.739+17C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2281+17C>A
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8444
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7341
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

6-157406059-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406059
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406059
    reference: chr 6
allele count: 1
allele frequency: 8.680555555555556e-6
allele num: 115200
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2068+20T>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.508+20T>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.140+20T>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.739+20T>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2281+20T>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2242+20T>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.350+20T>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2242+20T>G
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16676
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3132
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

6-157406063-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406063
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406063
    reference: chr 6
allele count: 3
allele frequency: 2.61798380340687e-5
allele num: 114592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2242+24T>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.350+24T>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2068+24T>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2281+24T>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2242+24T>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.739+24T>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.508+24T>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.140+24T>A
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8384
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5043
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4441
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1984
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

6-157406063-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406063
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406063
    reference: chr 6
allele count: 1
allele frequency: 8.726612678022898e-6
allele num: 114592
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.140+24T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.508+24T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2242+24T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.739+24T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2281+24T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2242+24T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.350+24T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2068+24T>C
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13439
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16368
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4441
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

6-157406079-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406079
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406079
    reference: chr 6
allele count: 5
allele frequency: 4.473232178643001e-5
allele num: 111776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.350+40A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.140+40A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.739+40A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2068+40A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2242+40A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2242+40A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2281+40A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.508+40A>G
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8139
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12573
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11977
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6347
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3200
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13940
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

6-157406090-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157406090
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157406090
    reference: chr 6
allele count: 1
allele frequency: 9.046007996671069e-6
allele num: 110546
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2281+51T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2242+51T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2068+51T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.350+51T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.739+51T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.140+51T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2242+51T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.508+51T>C
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10496
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1761
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3783
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1464
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4082
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

6-157431564-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431564
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431564
    reference: chr 6
allele count: 891
allele frequency: 7.435657776145809e-3
allele num: 119828
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.141-42A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2414T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2243-42A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.351-42A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2069-42A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2282-42A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22598A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2243-42A>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.509-42A>G
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10338
  bin: 3.25e1
  variant carriers: 152
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13153
  bin: 2.75e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 3.75e1
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 4.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 1.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 4.25e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 15195
  bin: 2.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2146
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6864
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4913
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 4
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

6-157431567-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431567
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431567
    reference: chr 6
allele count: 4
allele frequency: 3.337783711615487e-5
allele num: 119840
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.141-39G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2243-39G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2282-39G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2243-39G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22595G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2069-39G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.351-39G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2417C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.509-39G>T
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13385
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10631
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4238
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2965
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-157431571-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431571
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431570
    reference: chr 6
allele count: 1
allele frequency: 8.329723786359244e-6
allele num: 120052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22586delC
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2243-30delC
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2422delG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2282-30delC
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.141-30delC
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2243-30delC
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2069-30delC
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.509-30delC
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.351-30delC
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6038
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3642
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5092
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: TC
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-157431572-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431572
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431572
    reference: chr 6
allele count: 29
allele frequency: 2.414172022243681e-4
allele num: 120124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2243-34C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2282-34C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2422G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.141-34C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2243-34C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.351-34C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22590C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2069-34C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.509-34C>A
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6060
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16407
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11020
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13838
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18161
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2223
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

6-157431575-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431575
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431575
    reference: chr 6
allele count: 2
allele frequency: 1.662399840409615e-5
allele num: 120308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22587C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.141-31C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2069-31C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2243-31C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2243-31C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.509-31C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2425G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2282-31C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.351-31C>T
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11204
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3718
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

6-157431617-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431617
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431617
    reference: chr 6
allele count: 1
allele frequency: 8.260912665631299e-6
allele num: 121052
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2467G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.362C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2080C>T
  hgvsp: ENSP00000275248.4:p.Pro694Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2293C>T
  hgvsp: ENSP00000344546.4:p.Pro765Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2254C>T
  hgvsp: ENSP00000055163.7:p.Pro752Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.520C>T
  hgvsp: ENSP00000313006.6:p.Pro174Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.152C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2254C>T
  hgvsp: ENSP00000356116.1:p.Pro752Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22545C>T
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13230
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro765Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

6-157431621-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431621
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431621
    reference: chr 6
allele count: 4
allele frequency: 3.303819215012555e-5
allele num: 121072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.524C>T
  hgvsp: ENSP00000313006.6:p.Pro175Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22541C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.156C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2297C>T
  hgvsp: ENSP00000344546.4:p.Pro766Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2471G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.366C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2258C>T
  hgvsp: ENSP00000356116.1:p.Pro753Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2258C>T
  hgvsp: ENSP00000055163.7:p.Pro753Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2084C>T
  hgvsp: ENSP00000275248.4:p.Pro695Leu
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11553
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14934
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7778
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro766Leu
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

6-157431622-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431622
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431622
    reference: chr 6
allele count: 13
allele frequency: 1.073758982406872e-4
allele num: 121070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2085G>A
  hgvsp: ENST00000275248.4:c.2085G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.525G>A
  hgvsp: ENST00000319584.6:c.525G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22540G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2472C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2259G>A
  hgvsp: ENST00000367148.1:c.2259G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2298G>A
  hgvsp: ENST00000346085.5:c.2298G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2259G>A
  hgvsp: ENST00000350026.5:c.2259G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.157G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.367G>A
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3811
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro766Pro
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD

6-157431631-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431631
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431631
    reference: chr 6
allele count: 3
allele frequency: 2.476759737793703e-5
allele num: 121126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.534C>T
  hgvsp: ENST00000319584.6:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2094C>T
  hgvsp: ENST00000275248.4:c.2094C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2307C>T
  hgvsp: ENST00000346085.5:c.2307C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2268C>T
  hgvsp: ENST00000350026.5:c.2268C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2268C>T
  hgvsp: ENST00000367148.1:c.2268C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.166C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22531C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2481G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.376C>T
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3804
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2262
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro769Pro
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

6-157431636-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431636
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431636
    reference: chr 6
allele count: 2
allele frequency: 1.650764303872693e-5
allele num: 121156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2099G>A
  hgvsp: ENSP00000275248.4:p.Ser700Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2273G>A
  hgvsp: ENSP00000055163.7:p.Ser758Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2273G>A
  hgvsp: ENSP00000356116.1:p.Ser758Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2486C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.171G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22526G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2312G>A
  hgvsp: ENSP00000344546.4:p.Ser771Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.539G>A
  hgvsp: ENSP00000313006.6:p.Ser180Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.381G>A
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3816
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13232
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7791
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser771Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

6-157431654-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431654
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431654
    reference: chr 6
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2330C>T
  hgvsp: ENSP00000344546.4:p.Ser777Phe
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2291C>T
  hgvsp: ENSP00000356116.1:p.Ser764Phe
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.189C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.399C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22508C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.557C>T
  hgvsp: ENSP00000313006.6:p.Ser186Phe
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2504G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2117C>T
  hgvsp: ENSP00000275248.4:p.Ser706Phe
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2291C>T
  hgvsp: ENSP00000055163.7:p.Ser764Phe
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13234
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20637
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser777Phe
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-157431656-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431656
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431656
    reference: chr 6
allele count: 2
allele frequency: 1.649947201689546e-5
allele num: 121216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2119C>A
  hgvsp: ENSP00000275248.4:p.His707Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2293C>A
  hgvsp: ENSP00000356116.1:p.His765Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.559C>A
  hgvsp: ENSP00000313006.6:p.His187Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2293C>A
  hgvsp: ENSP00000055163.7:p.His765Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22506C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2506G>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2332C>A
  hgvsp: ENSP00000344546.4:p.His778Asn
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.401C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.191C>A
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13235
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3815
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20644
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His778Asn
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

6-157431659-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431659
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431659
    reference: chr 6
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.404C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2296C>T
  hgvsp: ENSP00000356116.1:p.Pro766Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2122C>T
  hgvsp: ENSP00000275248.4:p.Pro708Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.194C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2335C>T
  hgvsp: ENSP00000344546.4:p.Pro779Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22503C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2296C>T
  hgvsp: ENSP00000055163.7:p.Pro766Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.562C>T
  hgvsp: ENSP00000313006.6:p.Pro188Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2509G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4401
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3812
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro779Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

6-157431661-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431661
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431661
    reference: chr 6
allele count: 5
allele frequency: 4.124595789612618e-5
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2511G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.406C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2298C>T
  hgvsp: ENST00000367148.1:c.2298C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.196C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2337C>T
  hgvsp: ENST00000346085.5:c.2337C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2124C>T
  hgvsp: ENST00000275248.4:c.2124C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2298C>T
  hgvsp: ENST00000350026.5:c.2298C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.564C>T
  hgvsp: ENST00000319584.6:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22501C>T
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 20644
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro779Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

6-157431662-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431662
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431662
    reference: chr 6
allele count: 84
allele frequency: 6.929206605843631e-4
allele num: 121226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.197G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.565G>A
  hgvsp: ENSP00000313006.6:p.Ala189Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.407G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2125G>A
  hgvsp: ENSP00000275248.4:p.Ala709Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2299G>A
  hgvsp: ENSP00000055163.7:p.Ala767Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2512C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22500G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2299G>A
  hgvsp: ENSP00000356116.1:p.Ala767Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2338G>A
  hgvsp: ENSP00000344546.4:p.Ala780Thr
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11537
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17045
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 9.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5256
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4391
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala780Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

6-157431667-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431667
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431667
    reference: chr 6
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.412G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2343G>A
  hgvsp: ENST00000346085.5:c.2343G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2130G>A
  hgvsp: ENST00000275248.4:c.2130G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.570G>A
  hgvsp: ENST00000319584.6:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.202G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2304G>A
  hgvsp: ENST00000350026.5:c.2304G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2517C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2304G>A
  hgvsp: ENST00000367148.1:c.2304G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22495G>A
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3023
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3810
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu781Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP

6-157431673-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431673
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431673
    reference: chr 6
allele count: 2
allele frequency: 1.649647800194658e-5
allele num: 121238
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2523C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.418G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2310G>A
  hgvsp: ENST00000350026.5:c.2310G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.208G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2310G>A
  hgvsp: ENST00000367148.1:c.2310G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.576G>A
  hgvsp: ENST00000319584.6:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2136G>A
  hgvsp: ENST00000275248.4:c.2136G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22489G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2349G>A
  hgvsp: ENST00000346085.5:c.2349G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2261
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln783Gln
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

6-157431681-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431681
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431681
    reference: chr 6
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2357T>C
  hgvsp: ENSP00000344546.4:p.Met786Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2144T>C
  hgvsp: ENSP00000275248.4:p.Met715Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2531A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.584T>C
  hgvsp: ENSP00000313006.6:p.Met195Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2318T>C
  hgvsp: ENSP00000356116.1:p.Met773Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.426T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2318T>C
  hgvsp: ENSP00000055163.7:p.Met773Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.216T>C
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22481T>C
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17007
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met786Thr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-157431699-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431699
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431699
    reference: chr 6
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2549G>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2332+4C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2371+4C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22463C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2332+4C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2158+4C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.598+4C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.234C>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.440+4C>A
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3023
  bin: 9.25e1
  variant carriers: 0
hgvs: c.2371+4C>A
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP

6-157431699-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431699
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431699
    reference: chr 6
allele count: 3
allele frequency: 2.47496163809461e-5
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2158+4C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.440+4C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.598+4C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2332+4C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.234C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2371+4C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2332+4C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22463C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2549G>A
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11563
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2260
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
hgvs: c.2371+4C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

6-157431705-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431705
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431705
    reference: chr 6
allele count: 6
allele frequency: 4.949923276189219e-5
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2332+10C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.240C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2332+10C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.598+10C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22457C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2158+10C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.440+10C>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2555G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2371+10C>T
  variant of: http://identifiers.org/hgnc/18040
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4397
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7774
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20392
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

6-157431707-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431707
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431707
    reference: chr 6
allele count: 2
allele frequency: 1.650028875505322e-5
allele num: 121210
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2557C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2371+12G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.598+12G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2332+12G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.440+12G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2332+12G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22455G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.242G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2158+12G>A
  variant of: http://identifiers.org/hgnc/18040
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3022
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

6-157431707-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431707
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431707
    reference: chr 6
allele count: 5
allele frequency: 4.125072188763303e-5
allele num: 121210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.598+12G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2332+12G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2332+12G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2371+12G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.440+12G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2557C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.242G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22455G>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2158+12G>T
  variant of: http://identifiers.org/hgnc/18040
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3802
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2259
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

6-157431719-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431719
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431719
    reference: chr 6
allele count: 19
allele frequency: 1.567811994586923e-4
allele num: 121188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2332+24C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22443C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.440+24C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2158+24C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2569G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.254C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2371+24C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.598+24C>G
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2332+24C>G
  variant of: http://identifiers.org/hgnc/18040
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15050
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20120
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

6-157431720-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431720
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431720
    reference: chr 6
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22442A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000452544
  gene symbol: ARID1B
  hgvsc: ENST00000452544.1:n.440+25A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2570T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.255A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.2371+25A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2158+25A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.2332+25A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.2332+25A>T
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000313006
  ensembl transcript: ENST00000319584
  gene symbol: ARID1B
  hgvsc: ENST00000319584.6:c.598+25A>T
  variant of: http://identifiers.org/hgnc/18040
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3025
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

6-157431722-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157431722
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157431722
    reference: chr 6
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233044
  ensembl transcript: ENST00000442936
  gene symbol: RP1-137K2.2
  hgvsc: ENST00000442936.1:n.134-2572C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.740-22440G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049618
  ensembl transcript: ENST00000493658
  gene symbol: ARID1B
  hgvsc: ENST00000493658.1:n.257G>A
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.2158+27G>A
  variant of: http://identifiers.org/hgnc/18040
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
num of homozygotes: 0
reference allele: G

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

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

GenotypeQuality
all individuals: 1688
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 41489
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 1410
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3052
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
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: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 3.389348e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.353e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.97e-1

QD
type: SiteQuality
SIO_000300: 1.327e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 8768
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 909
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1364
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495459585818323e-5
allele num: 66734
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
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: 8646
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.762e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.389521e6

MQRankSum
type: SiteQuality
SIO_000300: 7.03e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.207e1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.85e-1

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3052
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8742
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.773e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.59e-1

DP
type: SiteQuality
SIO_000300: 3.38936e6

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.3e-2

QD
type: SiteQuality
SIO_000300: 1.201e1

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

GenotypeQuality
all individuals: 909
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1985
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41490
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1358
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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: 8652
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.159999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.591e-1

QD
type: SiteQuality
SIO_000300: 9.84e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

MQRankSum
type: SiteQuality
SIO_000300: -9.52e-1

DP
type: SiteQuality
SIO_000300: 3.389398e6

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41490
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 1361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8736
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.32e-1

DP
type: SiteQuality
SIO_000300: 3.38944e6

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

MQ
type: SiteQuality
SIO_000300: 5.989e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.79e-1

QD
type: SiteQuality
SIO_000300: 1.201e1

FS
type: SiteQuality
SIO_000300: 3.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.57e-1

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8692
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41498
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1984
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1686
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.049003446725611e-4
allele num: 66730
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.107e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 3.389742e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

QD
type: SiteQuality
SIO_000300: 1.389e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 8694
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41499
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1686
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 2.95e0

DP
type: SiteQuality
SIO_000300: 3.389669e6

QD
type: SiteQuality
SIO_000300: 1.004e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

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

GenotypeQuality
all individuals: 1
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
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

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

African
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allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.941e1

FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 6.82e-2

QD
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ClippingRankSum
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MQRankSum
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SIO_000300: -4.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.93e-1

ReadPosRankSum
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DP
type: SiteQuality
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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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South Asian
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allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.0459e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
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SIO_000300: 1.127e1

ReadPosRankSum
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BaseQRankSum
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SIO_000300: -2.772e0

MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

DP
type: SiteQuality
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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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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.69e-1

ClippingRankSum
type: SiteQuality
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VQSLOD
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 6.61e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.624277456647399e-4
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.754e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

VQSLOD
type: SiteQuality
SIO_000300: -2.259e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e-2

QD
type: SiteQuality
SIO_000300: 2.18e1

MQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

DP
type: SiteQuality
SIO_000300: 3.390244e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.74e-1

GenotypeQuality
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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
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GenotypeQuality
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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: 1410
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GenotypeQuality
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bin: 4.75e1
variant carriers: 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: 8648
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.045e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 3.390306e6

QD
type: SiteQuality
SIO_000300: 1.536e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 3.390916e6

FS
type: SiteQuality
SIO_000300: 2.477e0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 6.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 1.411e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

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: 9.75e1
variant carriers: 11

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 9
allele frequency: 8.650519031141869e-4
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.103e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.75e-1

QD
type: SiteQuality
SIO_000300: 1.241e1

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.75e-1

DP
type: SiteQuality
SIO_000300: 3.391585e6

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 13
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-1

QD
type: SiteQuality
SIO_000300: 1.694e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

FS
type: SiteQuality
SIO_000300: 1.164e0

DP
type: SiteQuality
SIO_000300: 3.391299e6

GenotypeQuality
all individuals: 10
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variant carriers: 5

GenotypeQuality
all individuals: 4
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variant carriers: 3

GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 502
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variant carriers: 25

GenotypeQuality
all individuals: 808
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GenotypeQuality
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GenotypeQuality
all individuals: 786
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GenotypeQuality
all individuals: 1922
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GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 48973
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GenotypeQuality
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GenotypeQuality
all individuals: 1271
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variant carriers: 20

GenotypeQuality
all individuals: 7
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variant carriers: 1

Other
type: Population
allele count: 433
allele frequency: 4.768722466960352e-1
allele num: 908
num of homozygotes: 114

East Asian
type: Population
allele count: 4784
allele frequency: 5.542168674698795e-1
allele num: 8632
num of homozygotes: 1312

African
type: Population
allele count: 3455
allele frequency: 3.321476639107864e-1
allele num: 10402
num of homozygotes: 561

European (Finnish)
type: Population
allele count: 2614
allele frequency: 3.955811138014528e-1
allele num: 6608
num of homozygotes: 534

European (Non-Finnish)
type: Population
allele count: 35167
allele frequency: 5.270991336670764e-1
allele num: 66718
num of homozygotes: 9344

South Asian
type: Population
allele count: 9358
allele frequency: 5.667393410852714e-1
allele num: 16512
num of homozygotes: 2681

Latino
type: Population
allele count: 7175
allele frequency: 6.201382886776146e-1
allele num: 11570
num of homozygotes: 2232

MQ
type: SiteQuality
SIO_000300: 5.962e1

VQSLOD
type: SiteQuality
SIO_000300: 4.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.67e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.019e1

DP
type: SiteQuality
SIO_000300: 5.813642e6

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: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 4.177e0

DP
type: SiteQuality
SIO_000300: 2.15922e6

MQ
type: SiteQuality
SIO_000300: 5.907e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 3.224e1

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.803e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

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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bin: 1.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

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

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

East Asian
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.211e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.71e-1

QD
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VQSLOD
type: SiteQuality
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FS
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InbreedingCoeff
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MQRankSum
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SIO_000300: -6.850000000000001e-1

ClippingRankSum
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SIO_000300: 4.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.158961e6

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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variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

FS
type: SiteQuality
SIO_000300: 4.605e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 3.135e1

DP
type: SiteQuality
SIO_000300: 2.15853e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.558e0

VQSLOD
type: SiteQuality
SIO_000300: -1.742e0

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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bin: 9.25e1
variant carriers: 0

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

East Asian
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allele count: 2
allele frequency: 2.313743637204998e-4
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99805126667666e-5
allele num: 66710
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.381e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.073e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.73e0

DP
type: SiteQuality
SIO_000300: 2.157598e6

MQ
type: SiteQuality
SIO_000300: 5.944e1

FS
type: SiteQuality
SIO_000300: 1.137e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-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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variant carriers: 0

Other
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allele num: 908
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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DP
type: SiteQuality
SIO_000300: 2.156799e6

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

European (Non-Finnish)
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allele frequency: 2.997422216893472e-5
allele num: 66724
num of homozygotes: 0

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

Other
type: Population
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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African
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East Asian
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MQ
type: SiteQuality
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MQRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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QD
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VQSLOD
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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Other
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allele num: 908
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

Latino
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South Asian
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allele num: 16512
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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QD
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FS
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
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Other
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African
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allele frequency: 0.0e0
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Latino
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South Asian
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East Asian
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allele frequency: 1.27285350613284e-3
allele num: 8642
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European (Finnish)
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQ
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DP
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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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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variant carriers: 0

Other
type: Population
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Latino
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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VQSLOD
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SIO_000300: 8.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

DP
type: SiteQuality
SIO_000300: 2.154463e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 5.969e0

BaseQRankSum
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SIO_000300: -1.8e0

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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variant carriers: 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: 66706
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8640
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South Asian
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allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.829e0

DP
type: SiteQuality
SIO_000300: 2.154178e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 0.0e0

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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South Asian
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allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.354e1

MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.974e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.153804e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.12e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16502
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: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99868058054456e-5
allele num: 66696
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.58e0

FS
type: SiteQuality
SIO_000300: 1.152e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 8.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.286e1

DP
type: SiteQuality
SIO_000300: 2.153497e6

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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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.014e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.212e1

DP
type: SiteQuality
SIO_000300: 2.152368e6

MQ
type: SiteQuality
SIO_000300: 5.932e1

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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variant carriers: 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: 11572
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.150788e6

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.906e1

VQSLOD
type: SiteQuality
SIO_000300: 2.12e-1

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.97e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.09979260705136e-5
allele num: 16394
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
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allele count: 0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.56e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508432135638218e-5
allele num: 66294
num of homozygotes: 0

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

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

African
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66254
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Latino
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Other
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
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MQRankSum
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MQ
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DP
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.217e0

VQSLOD
type: SiteQuality
SIO_000300: 7.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.11747e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.22e-1

QD
type: SiteQuality
SIO_000300: 1.496e1

GenotypeQuality
all individuals: 2283
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11589
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.598046978094485e-5
allele num: 15156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66076
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.917e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.269e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

QD
type: SiteQuality
SIO_000300: 1.643e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.969e-1

FS
type: SiteQuality
SIO_000300: 4.113e0

MQRankSum
type: SiteQuality
SIO_000300: -1.114e0

DP
type: SiteQuality
SIO_000300: 2.102005e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.624271330153684e-5
allele num: 15096
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66030
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.278e1

DP
type: SiteQuality
SIO_000300: 2.098999e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

GenotypeQuality
all individuals: 3124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1988
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.69414014953921e-5
allele num: 11502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13968
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.104447089704849e-5
allele num: 65526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

FS
type: SiteQuality
SIO_000300: 1.246e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

QD
type: SiteQuality
SIO_000300: 1.296e1

DP
type: SiteQuality
SIO_000300: 2.059159e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11574
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 326
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variant carriers: 0

GenotypeQuality
all individuals: 7397
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variant carriers: 0

GenotypeQuality
all individuals: 485
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variant carriers: 0

GenotypeQuality
all individuals: 49
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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
all individuals: 3124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17572
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13408
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.873617693522907e-5
allele num: 10128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.109e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.414e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

QD
type: SiteQuality
SIO_000300: 1.409e1

VQSLOD
type: SiteQuality
SIO_000300: -2.543e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.14e0

DP
type: SiteQuality
SIO_000300: 2.044779e6

MQ
type: SiteQuality
SIO_000300: 5.907e1

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4170
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 120
bin: 4.75e1
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: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17328
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10094
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65224
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

DP
type: SiteQuality
SIO_000300: 2.038831e6

QD
type: SiteQuality
SIO_000300: 1.041e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.39e-1

FS
type: SiteQuality
SIO_000300: 1.694e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.74e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 562
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.705347511172754e-5
allele num: 12978
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65144
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: 10074
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.532e0

VQSLOD
type: SiteQuality
SIO_000300: -2.067e-1

QD
type: SiteQuality
SIO_000300: 7.76e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

DP
type: SiteQuality
SIO_000300: 2.033925e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 140
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GenotypeQuality
all individuals: 4556
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GenotypeQuality
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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
all individuals: 4160
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10054
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.878978884336589e-5
allele num: 12692
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65030
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: 854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.024872e6

VQSLOD
type: SiteQuality
SIO_000300: -1.211e-1

FS
type: SiteQuality
SIO_000300: 5.137e0

MQRankSum
type: SiteQuality
SIO_000300: -1.444e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

QD
type: SiteQuality
SIO_000300: 1.212e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.74e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3115
bin: 9.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 213
bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.543586109142452e-4
allele num: 8466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64864
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10028
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12312
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

QD
type: SiteQuality
SIO_000300: 1.24e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 2.014989e6

GenotypeQuality
all individuals: 213
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7175
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3105
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11562
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3115
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variant carriers: 0

GenotypeQuality
all individuals: 1984
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variant carriers: 0

GenotypeQuality
all individuals: 4157
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.75e1
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GenotypeQuality
all individuals: 5043
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GenotypeQuality
all individuals: 654
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.122157244964262e-5
allele num: 12312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64864
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

VQSLOD
type: SiteQuality
SIO_000300: 4.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 2.014989e6

QD
type: SiteQuality
SIO_000300: 1.24e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1634
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1327
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3099
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4940
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4113
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2953
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11544
bin: 9.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.798365462599039e-5
allele num: 64116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 1.349e1

FS
type: SiteQuality
SIO_000300: 7.458e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.29e-1

DP
type: SiteQuality
SIO_000300: 1.957707e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -9.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

GenotypeQuality
all individuals: 811
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11530
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1586
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2117
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6055
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4822
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2845
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3095
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56907048264608e-5
allele num: 63732
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.92351e6

MQRankSum
type: SiteQuality
SIO_000300: -1.297e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.302e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.845e1

VQSLOD
type: SiteQuality
SIO_000300: -4.434e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e0

QD
type: SiteQuality
SIO_000300: 9.52e0

GenotypeQuality
all individuals: 1127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 210
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15826
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 859
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3466
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 999
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13746
bin: 9.75e1
variant carriers: 880

GenotypeQuality
all individuals: 552
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 3
allele frequency: 3.355704697986577e-3
allele num: 894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 20
allele frequency: 3.057169061449098e-3
allele num: 6542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 789
allele frequency: 1.196869027031947e-2
allele num: 65922
num of homozygotes: 4

Latino
type: Population
allele count: 41
allele frequency: 3.59207990187489e-3
allele num: 11414
num of homozygotes: 0

African
type: Population
allele count: 31
allele frequency: 3.040408003138486e-3
allele num: 10196
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.284490145672665e-4
allele num: 16338
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.298e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

QD
type: SiteQuality
SIO_000300: 1.35e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.908906e6

GenotypeQuality
all individuals: 7009
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1067
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16986
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5001
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2208
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3544
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13171
bin: 9.75e1
variant carriers: 4

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.060912151821243e-4
allele num: 6534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.033980582524272e-5
allele num: 65920
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.77e-1

DP
type: SiteQuality
SIO_000300: 1.922403e6

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

MQ
type: SiteQuality
SIO_000300: 5.946e1

FS
type: SiteQuality
SIO_000300: 6.995e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.563e0

QD
type: SiteQuality
SIO_000300: 1.522e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.44e-1

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17887
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2227
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7275
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13191
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 750
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2990
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4291
bin: 8.25e1
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: 8.739730816290858e-5
allele num: 11442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66030
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

FS
type: SiteQuality
SIO_000300: 5.393e0

QD
type: SiteQuality
SIO_000300: 9.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

MQ
type: SiteQuality
SIO_000300: 6.087e1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 1.937911e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e0

GenotypeQuality
all individuals: 5084
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4293
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13210
bin: 9.75e1
variant carriers: 29

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3631
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2987
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7283
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

South Asian
type: Population
allele count: 28
allele frequency: 1.710236989982898e-3
allele num: 16372
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514187941007238e-5
allele num: 66042
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e-1

QD
type: SiteQuality
SIO_000300: 1.341e1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.952e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.942717e6

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5161
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18967
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7461
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13215
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 248
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3003
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4329
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.023431594860166e-5
allele num: 66150
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.301e1

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

DP
type: SiteQuality
SIO_000300: 1.952809e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.74e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeQuality
all individuals: 5263
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3018
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7768
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20450
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2263
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3808
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4401
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502268425322237e-5
allele num: 66566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 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: 16488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.777e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.509e0

VQSLOD
type: SiteQuality
SIO_000300: -2.126e0

DP
type: SiteQuality
SIO_000300: 1.977527e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

MQRankSum
type: SiteQuality
SIO_000300: -2.161e0

QD
type: SiteQuality
SIO_000300: 1.284e1

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3810
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5264
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 202
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3019
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20454
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4400
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13232
bin: 9.75e1
variant carriers: 4

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

South Asian
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allele frequency: 0.0e0
allele num: 16488
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Latino
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allele count: 2
allele frequency: 1.733102253032929e-4
allele num: 11540
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.004266057802079e-5
allele num: 66572
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 904
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European (Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 6.45e-1

DP
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QD
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MQ
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VQSLOD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -3.18e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 904
num of homozygotes: 0

East Asian
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allele count: 11
allele frequency: 1.272559000462749e-3
allele num: 8644
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.502268425322237e-5
allele num: 66566
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11542
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10316
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South Asian
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allele frequency: 6.064281382656155e-5
allele num: 16490
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VQSLOD
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MQ
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16498
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
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: 6606
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.731002250302925e-4
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50159168718842e-5
allele num: 66596
num of homozygotes: 0

InbreedingCoeff
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BaseQRankSum
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MQ
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QD
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VQSLOD
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SIO_000300: 1.56e-1

ReadPosRankSum
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ClippingRankSum
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FS
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MQRankSum
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

African
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: 904
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.66e0

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

BaseQRankSum
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FS
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VQSLOD
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QD
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

Other
type: Population
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East Asian
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.96e-1

InbreedingCoeff
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BaseQRankSum
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QD
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ClippingRankSum
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SIO_000300: -5.42e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

MQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 906
num of homozygotes: 0

European (Finnish)
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allele frequency: 1.511944360447536e-4
allele num: 6614
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African
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

East Asian
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Latino
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allele count: 0
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num of homozygotes: 0

MQ
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SIO_000300: 6.0e1

FS
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ClippingRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

European (Finnish)
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Other
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African
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Latino
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East Asian
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South Asian
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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allele frequency: 5.78168362627197e-4
allele num: 8648
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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Other
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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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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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 71
allele frequency: 1.065234351557343e-3
allele num: 66652
num of homozygotes: 0

European (Finnish)
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Other
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South Asian
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allele frequency: 3.635041802980734e-4
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East Asian
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African
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allele frequency: 9.671179883945841e-5
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Latino
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allele frequency: 5.190311418685121e-4
allele num: 11560
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FS
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.53e0

DP
type: SiteQuality
SIO_000300: 1.987196e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.21e0

QD
type: SiteQuality
SIO_000300: 1.134e1

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

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5263
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7799
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20636
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2260
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13247
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
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: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.108e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.197e1

MQRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

FS
type: SiteQuality
SIO_000300: 6.181e0

DP
type: SiteQuality
SIO_000300: 1.981759e6

GenotypeQuality
all individuals: 118
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7796
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3809
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5261
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4400
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
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: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.934610176049526e-4
allele num: 10338
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.844e0

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

QD
type: SiteQuality
SIO_000300: 1.028e1

DP
type: SiteQuality
SIO_000300: 1.981856e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.620000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e-1

GenotypeQuality
all individuals: 2261
bin: 8.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 20610
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4401
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13246
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3810
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7795
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3024
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.92e1

QD
type: SiteQuality
SIO_000300: 1.512e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.981771e6

VQSLOD
type: SiteQuality
SIO_000300: 3.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.151e0

GenotypeQuality
all individuals: 20501
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7776
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5260
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
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variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4402
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13247
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.669309611293753e-5
allele num: 10342
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: 11560
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
SIO_000300: 1.427e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

DP
type: SiteQuality
SIO_000300: 1.981131e6

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

GenotypeQuality
all individuals: 4402
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3806
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20501
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5260
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variant carriers: 0

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

GenotypeQuality
all individuals: 13247
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 7776
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3023
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000840235265874e-5
allele num: 66648
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: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.29e0

MQRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.427e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.69e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

DP
type: SiteQuality
SIO_000300: 1.981131e6

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2259
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 13250
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 62
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3800
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3023
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.029935765361775e-4
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.7e-1

FS
type: SiteQuality
SIO_000300: 1.136e0

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 1.980594e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.616e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.23e-1

QD
type: SiteQuality
SIO_000300: 1.151e1

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

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3802
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20421
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212121212121212e-4
allele num: 16500
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: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.977e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.25e-1

QD
type: SiteQuality
SIO_000300: 1.29e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.515e0

DP
type: SiteQuality
SIO_000300: 1.980588e6

VQSLOD
type: SiteQuality
SIO_000300: 4.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e-1

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3022
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13248
bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20421
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7772
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.501875468867217e-5
allele num: 66650
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.25e-1

DP
type: SiteQuality
SIO_000300: 1.980588e6

FS
type: SiteQuality
SIO_000300: 1.65e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.29e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.515e0

GenotypeQuality
all individuals: 5248
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13257
bin: 9.75e1
variant carriers: 19

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

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

GenotypeQuality
all individuals: 137
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3024
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7731
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4396
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3793
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 19
allele frequency: 2.197547999074717e-3
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66636
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 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: 16494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.038e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.14e0

QD
type: SiteQuality
SIO_000300: 1.516e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.979263e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
all individuals: 157
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2256
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20120
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3799
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7742
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5248
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13249
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
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: 8646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.27e-1

FS
type: SiteQuality
SIO_000300: 6.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.258e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.17e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

DP
type: SiteQuality
SIO_000300: 1.978354e6