11-69996033-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69996033
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69996033
    reference: chr 11
allele count: 3
allele frequency: 2.149305058031236e-4
allele num: 13958
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1341+135T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.72+135T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.546+135T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1257+135T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.993+135T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.993+135T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1353+29T>C
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28673
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8002
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1791
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1393
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

11-69996037-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69996037
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69996037
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 14602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.72+139C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1257+139C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.993+139C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1341+139C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1353+33C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.993+139C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.546+139C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28024
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23129
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1749
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/11-69996039-A-ACCCCCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69996039
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69996046
    reference: chr 11
allele count: 1
allele frequency: 9.135757354284671e-5
allele num: 10946
alternate allele: ACCCCCCC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1353+40_1353+41insCCCCCCC
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16929
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 13464
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 2.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-69996039-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69996039
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69996039
    reference: chr 11
allele count: 79
allele frequency: 7.217248309884889e-3
allele num: 10946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.993+141A>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1257+141A>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.546+141A>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.72+141A>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1341+141A>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1353+35A>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.993+141A>C
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 1.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26269
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 7.5e0
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 3.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 1.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 2.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 5.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 5.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13464
  bin: 7.5e0
  variant carriers: 5
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-69996042-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69996042
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69996042
    reference: chr 11
allele count: 1
allele frequency: 6.999860002799944e-5
allele num: 14286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.546+144C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.993+144C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.993+144C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1353+38C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1341+144C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.72+144C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1257+144C>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5840
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1832
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1661
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD

11-69996042-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69996042
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69996042
    reference: chr 11
allele count: 1
allele frequency: 6.999860002799944e-5
allele num: 14286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.993+144C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.993+144C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1353+38C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.546+144C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1341+144C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.72+144C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1257+144C>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5840
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

11-69998510-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998510
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998510
    reference: chr 11
allele count: 3
allele frequency: 3.090553209024416e-5
allele num: 97070
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-653A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-653A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-653A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.73-46A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.547-46A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-653A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1342-46A>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9437
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1282
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6253
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2942
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

11-69998512-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998512
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998512
    reference: chr 11
allele count: 2
allele frequency: 2.057316847367663e-5
allele num: 97214
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.73-44T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-651T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-651T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.547-44T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-651T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-651T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1342-44T>C
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1605
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6728
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9449
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

11-69998518-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998518
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998518
    reference: chr 11
allele count: 1
allele frequency: 1.02604091851183e-5
allele num: 97462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.73-38C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-645C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-645C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-645C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1342-38C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-645C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.547-38C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14129
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1882
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2212
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2289
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

11-69998524-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998524
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998524
    reference: chr 11
allele count: 1
allele frequency: 1.018661885746883e-5
allele num: 98168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.547-32G>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.73-32G>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-639G>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-639G>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1342-32G>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-639G>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-639G>C
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9442
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3913
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6174
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4760
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-69998530-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998530
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998530
    reference: chr 11
allele count: 4
allele frequency: 4.052849152954527e-5
allele num: 98696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.547-26G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-633G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-633G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1342-26G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-633G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-633G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.73-26G>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3717
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17555
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ

11-69998536-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998536
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998536
    reference: chr 11
allele count: 11
allele frequency: 1.105261042562598e-4
allele num: 99524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-627A>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-627A>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-627A>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.547-20A>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1342-20A>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.73-20A>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-627A>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 20210
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10072
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3435
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1091
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1501
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1888
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10256
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3508
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

11-69998537-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998537
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998537
    reference: chr 11
allele count: 2
allele frequency: 2.004449878730782e-5
allele num: 99778
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-626C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-626C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.73-19C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-626C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1342-19C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.547-19C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-626C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 20458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2059
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5034
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3304
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

11-69998538-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998538
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998538
    reference: chr 11
allele count: 1
allele frequency: 9.990209594597294e-6
allele num: 100098
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1342-18T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.547-18T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-625T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-625T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.73-18T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-625T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-625T>C
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20726
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9929
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10257
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4939
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2116
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1768
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9460
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-69998546-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998546
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998546
    reference: chr 11
allele count: 2
allele frequency: 1.957138663274293e-5
allele num: 102190
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-617T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.73-10T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-617T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-617T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1342-10T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.547-10T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-617T>C
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2281
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3933
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

11-69998547-TCCCTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998547
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998542
    reference: chr 11
allele count: 1
allele frequency: 9.753242953281967e-6
allele num: 102530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-615_1258-611delCCCTG
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.73-8_73-4delCCCTG
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.547-8_547-4delCCCTG
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-615_1354-611delCCCTG
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-615_994-611delCCCTG
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1342-8_1342-4delCCCTG
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-615_994-611delCCCTG
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8860
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3790
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2303
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9639
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2160
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
hgvs: c.1342-8_1342-4delCCCTG
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: TCCCTG
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

11-69998558-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998558
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998558
    reference: chr 11
allele count: 2
allele frequency: 1.896993265673907e-5
allele num: 105430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-605G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1344G>A
  hgvsp: ENST00000355303.5:c.1344G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-605G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.549G>A
  hgvsp: ENST00000531349.1:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-605G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-605G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.75G>A
  hgvsp: ENST00000531300.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27132
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5357
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7015
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2430
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2864
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
hgvs: c.1344G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

11-69998575-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998575
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998575
    reference: chr 11
allele count: 1
allele frequency: 9.274201027581474e-6
allele num: 107826
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-588A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1353+8A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.84+8A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-588A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-588A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.558+8A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-588A>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26400
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2579
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8340
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
hgvs: c.1353+8A>G
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD

11-69998576-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998576
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998576
    reference: chr 11
allele count: 1
allele frequency: 9.276437847866419e-6
allele num: 107800
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.558+9C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-587C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1353+9C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-587C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-587C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-587C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.84+9C>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9465
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8406
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1819
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24888
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum

11-69998584-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998584
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998584
    reference: chr 11
allele count: 1
allele frequency: 9.241802521163728e-6
allele num: 108204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-579C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.84+17C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-579C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-579C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1353+17C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.558+17C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-579C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6237
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7824
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3513
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9467
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8473
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2671
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2159
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-69998585-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998585
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998585
    reference: chr 11
allele count: 309
allele frequency: 2.852553450758835e-3
allele num: 108324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.558+18G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.84+18G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1353+18G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-578G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-578G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-578G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-578G>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 1.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 5901
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 3.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 23828
  bin: 2.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 1.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 2.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2461
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2692
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2256
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3579
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8441
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 9
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

11-69998589-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998589
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998589
    reference: chr 11
allele count: 1
allele frequency: 9.21438180712456e-6
allele num: 108526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-574C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-574C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-574C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1353+22C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.84+22C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.558+22C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-574C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2701
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2858
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3972
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

11-69998590-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998590
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998590
    reference: chr 11
allele count: 4
allele frequency: 3.682088480586188e-5
allele num: 108634
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-573T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-573T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.558+23T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1353+23T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.84+23T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-573T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-573T>C
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6393
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22603
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2686
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3963
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2833
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24024
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

11-69998598-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998598
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998598
    reference: chr 11
allele count: 9
allele frequency: 8.281040098636389e-5
allele num: 108682
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.558+31C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-565C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-565C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1353+31C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.84+31C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-565C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-565C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5720
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6228
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8901
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8615
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20281
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9473
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4758
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3853
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-69998610-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69998610
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69998610
    reference: chr 11
allele count: 1
allele frequency: 9.216419973825367e-6
allele num: 108502
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.558+43C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-553C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1353+43C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-553C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.84+43C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-553C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-553C>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2734
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12473
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1852
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9469
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-69999116-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999116
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999116
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 49654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-47G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.85-47G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1354-47G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.559-47G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-47G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-47G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-47G>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25995
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6314
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2831
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1761
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4070
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4956
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/11-69999122-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999122
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999122
    reference: chr 11
allele count: 42841
allele frequency: 7.072039354221005e-1
allele num: 60578
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-41A>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-41A>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-41A>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.85-41A>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1354-41A>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-41A>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.559-41A>C
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 9.75e1
  variant carriers: 398
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 213
genotype depth: GenotypeDepth
  all individuals: 23184
  bin: 7.5e0
  variant carriers: 18324
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 2.25e1
  variant carriers: 1973
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.25e1
  variant carriers: 1545
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 330
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 14965
  bin: 1.25e1
  variant carriers: 13756
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 3.75e1
  variant carriers: 1194
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 898
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.25e1
  variant carriers: 445
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 2.5e0
  variant carriers: 2542
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 1.75e1
  variant carriers: 4389
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 2.75e1
  variant carriers: 1651
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 653
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 373
genotype quality: GenotypeQuality
  all individuals: 2856
  bin: 2.75e1
  variant carriers: 2563
genotype quality: GenotypeQuality
  all individuals: 4236
  bin: 3.25e1
  variant carriers: 3883
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 4.75e1
  variant carriers: 1490
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 5.25e1
  variant carriers: 1237
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 6.25e1
  variant carriers: 969
genotype quality: GenotypeQuality
  all individuals: 3689
  bin: 2.5e0
  variant carriers: 170
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 947
genotype quality: GenotypeQuality
  all individuals: 2068
  bin: 7.5e0
  variant carriers: 1093
genotype quality: GenotypeQuality
  all individuals: 4742
  bin: 1.75e1
  variant carriers: 4313
genotype quality: GenotypeQuality
  all individuals: 2065
  bin: 1.25e1
  variant carriers: 1601
num of homozygotes: 14795
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

11-69999128-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999128
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999128
    reference: chr 11
allele count: 1
allele frequency: 1.682821755519655e-5
allele num: 59424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-35A>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-35A>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.85-35A>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-35A>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1354-35A>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.559-35A>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-35A>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24169
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4639
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19458
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4861
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2745
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3255
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 4.25e1
  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: A
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

11-69999135-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999135
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999135
    reference: chr 11
allele count: 5
allele frequency: 8.332500083325001e-5
allele num: 60006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-28C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.85-28C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-28C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1354-28C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-28C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.559-28C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-28C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24645
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13917
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4382
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2507
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4306
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5296
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 9.25e1
  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: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

11-69999136-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999136
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999136
    reference: chr 11
allele count: 1
allele frequency: 1.65953068472236e-5
allele num: 60258
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.85-27T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1354-27T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-27T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-27T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-27T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.559-27T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-27T>C
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13886
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5283
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4285
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4864
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2355
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 956
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

11-69999149-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999149
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999149
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 61870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.85-14G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-14G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.559-14G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-14G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1354-14G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-14G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-14G>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25748
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6878
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3063
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4870
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26142
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2192
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

11-69999150-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999150
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999150
    reference: chr 11
allele count: 2
allele frequency: 3.215847697453049e-5
allele num: 62192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.85-13G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-13G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1354-13G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-13G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.559-13G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-13G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-13G>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26306
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4872
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum

11-69999156-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999156
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999156
    reference: chr 11
allele count: 1
allele frequency: 1.572772168223711e-5
allele num: 63582
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354-7T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.559-7T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.85-7T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994-7T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258-7T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1354-7T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994-7T>C
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8827
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2442
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3849
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4873
  bin: 9.75e1
  variant carriers: 1
hgvs: c.1354-7T>C
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

11-69999163-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999163
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999163
    reference: chr 11
allele count: 1
allele frequency: 1.521236460995497e-5
allele num: 65736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.559G>T
  hgvsp: ENSP00000432843.1:p.Asp187Tyr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.85G>T
  hgvsp: ENSP00000435868.1:p.Asp29Tyr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1258G>T
  hgvsp: ENSP00000319477.5:p.Asp420Tyr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.994G>T
  hgvsp: ENSP00000381551.2:p.Asp332Tyr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1354G>T
  hgvsp: ENSP00000347454.5:p.Asp452Tyr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1354G>T
  hgvsp: ENSP00000444689.1:p.Asp452Tyr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.994G>T
  hgvsp: ENSP00000435797.1:p.Asp332Tyr
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25181
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4877
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1393
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp452Tyr
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

11-69999166-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999166
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999166
    reference: chr 11
allele count: 5
allele frequency: 7.505478999669759e-5
allele num: 66618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.562C>T
  hgvsp: ENSP00000432843.1:p.His188Tyr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1357C>T
  hgvsp: ENSP00000347454.5:p.His453Tyr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.88C>T
  hgvsp: ENSP00000435868.1:p.His30Tyr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.997C>T
  hgvsp: ENSP00000381551.2:p.His333Tyr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1261C>T
  hgvsp: ENSP00000319477.5:p.His421Tyr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.997C>T
  hgvsp: ENSP00000435797.1:p.His333Tyr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1357C>T
  hgvsp: ENSP00000444689.1:p.His453Tyr
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10013
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1354
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26457
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4880
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His453Tyr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP

11-69999183-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999183
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999183
    reference: chr 11
allele count: 4
allele frequency: 5.599260897561522e-5
allele num: 71438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1014C>T
  hgvsp: ENST00000398543.2:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1014C>T
  hgvsp: ENST00000530676.1:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1278C>T
  hgvsp: ENST00000316296.5:c.1278C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.579C>T
  hgvsp: ENST00000531349.1:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1374C>T
  hgvsp: ENST00000355303.5:c.1374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.105C>T
  hgvsp: ENST00000531300.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1374C>T
  hgvsp: ENST00000538023.1:c.1374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22987
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9069
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13828
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1364
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25392
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr458Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

11-69999187-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999187
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999187
    reference: chr 11
allele count: 1
allele frequency: 1.373701851750096e-5
allele num: 72796
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.109G>A
  hgvsp: ENSP00000435868.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1378G>A
  hgvsp: ENSP00000347454.5:p.Ala460Thr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.583G>A
  hgvsp: ENSP00000432843.1:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1018G>A
  hgvsp: ENSP00000381551.2:p.Ala340Thr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1378G>A
  hgvsp: ENSP00000444689.1:p.Ala460Thr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1282G>A
  hgvsp: ENSP00000319477.5:p.Ala428Thr
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1018G>A
  hgvsp: ENSP00000435797.1:p.Ala340Thr
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2876
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25204
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1281
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala460Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

11-69999187-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999187
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999187
    reference: chr 11
allele count: 2
allele frequency: 2.747403703500192e-5
allele num: 72796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1282G>T
  hgvsp: ENSP00000319477.5:p.Ala428Ser
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1378G>T
  hgvsp: ENSP00000444689.1:p.Ala460Ser
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1018G>T
  hgvsp: ENSP00000435797.1:p.Ala340Ser
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.583G>T
  hgvsp: ENSP00000432843.1:p.Ala195Ser
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.109G>T
  hgvsp: ENSP00000435868.1:p.Ala37Ser
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1018G>T
  hgvsp: ENSP00000381551.2:p.Ala340Ser
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1378G>T
  hgvsp: ENSP00000347454.5:p.Ala460Ser
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14676
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9107
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2876
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25204
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala460Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

11-69999193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999193
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999193
    reference: chr 11
allele count: 5
allele frequency: 6.751100429369987e-5
allele num: 74062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.115G>A
  hgvsp: ENSP00000435868.1:p.Val39Ile
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1288G>A
  hgvsp: ENSP00000319477.5:p.Val430Ile
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1384G>A
  hgvsp: ENSP00000347454.5:p.Val462Ile
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1024G>A
  hgvsp: ENSP00000435797.1:p.Val342Ile
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1384G>A
  hgvsp: ENSP00000444689.1:p.Val462Ile
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1024G>A
  hgvsp: ENSP00000381551.2:p.Val342Ile
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.589G>A
  hgvsp: ENSP00000432843.1:p.Val197Ile
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9369
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14803
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2591
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val462Ile
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

11-69999207-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999207
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999207
    reference: chr 11
allele count: 1
allele frequency: 1.330778239114234e-5
allele num: 75144
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.603T>G
  hgvsp: ENST00000531349.1:c.603T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1302T>G
  hgvsp: ENST00000316296.5:c.1302T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.129T>G
  hgvsp: ENST00000531300.1:c.129T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1398T>G
  hgvsp: ENST00000355303.5:c.1398T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1038T>G
  hgvsp: ENST00000398543.2:c.1038T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1398T>G
  hgvsp: ENST00000538023.1:c.1398T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1038T>G
  hgvsp: ENST00000530676.1:c.1038T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4881
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3197
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12830
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser466Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

11-69999238-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999238
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999238
    reference: chr 11
allele count: 1
allele frequency: 1.346837625255899e-5
allele num: 74248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.156+4T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1425+4T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1425+4T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.630+4T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1329+4T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1065+4T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1065+4T>C
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3227
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4887
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4178
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22332
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1425+4T>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-69999239-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999239
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999239
    reference: chr 11
allele count: 3
allele frequency: 4.044216770018873e-5
allele num: 74180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.630+5G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1065+5G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1425+5G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1425+5G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1065+5G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1329+5G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.156+5G>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7599
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14312
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20281
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4153
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22510
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5353
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2072
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3358
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5085
  bin: 6.25e1
  variant carriers: 0
hgvs: c.1425+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

11-69999247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999247
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999247
    reference: chr 11
allele count: 1
allele frequency: 1.37438152831226e-5
allele num: 72760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1329+13C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1065+13C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.630+13C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1065+13C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1425+13C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1425+13C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.156+13C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7542
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3517
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3952
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5492
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3610
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3566
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2430
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

11-69999252-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999252
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999252
    reference: chr 11
allele count: 57572
allele frequency: 7.061969481379716e-1
allele num: 81524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.630+18G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1329+18G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1065+18G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1425+18G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1425+18G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.156+18G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1065+18G>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15630
  bin: 7.5e0
  variant carriers: 11894
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.75e1
  variant carriers: 1305
genotype depth: GenotypeDepth
  all individuals: 18024
  bin: 1.25e1
  variant carriers: 16348
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 4.75e1
  variant carriers: 1195
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.75e1
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 2.25e1
  variant carriers: 2959
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 3.25e1
  variant carriers: 1114
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 6.75e1
  variant carriers: 401
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 2.5e0
  variant carriers: 1092
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 237
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.75e1
  variant carriers: 733
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 4.25e1
  variant carriers: 1203
genotype depth: GenotypeDepth
  all individuals: 8914
  bin: 1.75e1
  variant carriers: 8618
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.25e1
  variant carriers: 554
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 310
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 9.75e1
  variant carriers: 835
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 245
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 5.25e1
  variant carriers: 983
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 3.75e1
  variant carriers: 1210
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 5.25e1
  variant carriers: 1799
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 5.75e1
  variant carriers: 948
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 9.25e1
  variant carriers: 1021
genotype quality: GenotypeQuality
  all individuals: 2593
  bin: 1.75e1
  variant carriers: 2399
genotype quality: GenotypeQuality
  all individuals: 1790
  bin: 6.25e1
  variant carriers: 1150
genotype quality: GenotypeQuality
  all individuals: 6072
  bin: 2.25e1
  variant carriers: 3395
genotype quality: GenotypeQuality
  all individuals: 2344
  bin: 2.75e1
  variant carriers: 2104
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 859
genotype quality: GenotypeQuality
  all individuals: 2385
  bin: 4.75e1
  variant carriers: 2367
genotype quality: GenotypeQuality
  all individuals: 4050
  bin: 3.25e1
  variant carriers: 3813
num of homozygotes: 19631
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

11-69999271-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999271
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999271
    reference: chr 11
allele count: 1
allele frequency: 2.026999635140066e-5
allele num: 49334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1425+37A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1065+37A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1065+37A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1425+37A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.630+37A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1329+37A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.156+37A>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11084
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23943
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2896
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4289
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11940
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5282
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3199
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

11-69999274-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999274
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999274
    reference: chr 11
allele count: 1
allele frequency: 2.092312842616228e-5
allele num: 47794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1425+40A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1065+40A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.630+40A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.156+40A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1425+40A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1329+40A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1065+40A>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11153
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11264
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5193
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12161
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1408
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17740
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5910
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2895
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

11-69999275-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69999275
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 69999275
    reference: chr 11
allele count: 9
allele frequency: 1.92348792477025e-4
allele num: 46790
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1065+41C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.630+41C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.156+41C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1329+41C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1065+41C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1425+41C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1425+41C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10809
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11149
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24955
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1169
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2740
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6230
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12160
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16461
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2887
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

11-70001968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70001968
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70001968
    reference: chr 11
allele count: 2
allele frequency: 9.763718023823472e-5
allele num: 20484
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-49C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1085C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-49C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1085C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1085C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1085C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1085C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2116
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

11-70001969-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70001969
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70001969
    reference: chr 11
allele count: 2
allele frequency: 9.765625000000001e-5
allele num: 20480
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1084G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1084G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1084G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1084G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1084G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-48G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-48G>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

11-70001969-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70001969
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70001969
    reference: chr 11
allele count: 1
allele frequency: 4.8828125e-5
allele num: 20480
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1084G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-48G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-48G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1084G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1084G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1084G>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1084G>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5909
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

11-70001975-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70001975
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70001975
    reference: chr 11
allele count: 34
allele frequency: 1.655629139072848e-3
allele num: 20536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1078C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1078C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-42C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1078C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1078C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-42C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1078C>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2183
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 2
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

11-70001976-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70001976
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70001976
    reference: chr 11
allele count: 13731
allele frequency: 6.612887690233096e-1
allele num: 20764
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-41A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1077A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1077A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1077A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1077A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-41A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1077A>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.25e1
  variant carriers: 620
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 2.25e1
  variant carriers: 335
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 420
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 3.75e1
  variant carriers: 720
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 5.75e1
  variant carriers: 766
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 4.25e1
  variant carriers: 796
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 2.75e1
  variant carriers: 421
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.25e1
  variant carriers: 444
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 4.75e1
  variant carriers: 801
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.5e0
  variant carriers: 537
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 288
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 633
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 653
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 2.5e0
  variant carriers: 453
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 5.25e1
  variant carriers: 834
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 248
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 342
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 179
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 546
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 86
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 6.75e1
  variant carriers: 79
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 7.5e0
  variant carriers: 291
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.25e1
  variant carriers: 95
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.75e1
  variant carriers: 100
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.25e1
  variant carriers: 130
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.25e1
  variant carriers: 151
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.75e1
  variant carriers: 88
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.75e1
  variant carriers: 181
num of homozygotes: 4572
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

11-70001979-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70001979
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70001979
    reference: chr 11
allele count: 2
allele frequency: 9.640412609659693e-5
allele num: 20746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1074T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1074T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-38T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1074T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1074T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1074T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-38T>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2431
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4229
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/11-70002005-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002005
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002006
    reference: chr 11
allele count: 6
allele frequency: 2.887947631882942e-4
allele num: 20776
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-5dupC
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1041dupC
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1041dupC
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1041dupC
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1041dupC
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1041dupC
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-5dupC
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3366
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2153
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-70002005-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002005
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002004
    reference: chr 11
allele count: 2
allele frequency: 9.626492106276473e-5
allele num: 20776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-5delC
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1041delC
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1041delC
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1041delC
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1041delC
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1041delC
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-5delC
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3366
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4208
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: AC
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

http://identifiers.org/exac.variant/11-70002009-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002009
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002009
    reference: chr 11
allele count: 3
allele frequency: 1.436919245138423e-4
allele num: 20878
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1044C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1044C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-8C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1044C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1044C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-8C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1044C>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4225
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2446
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1426-8C>A
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

11-70002009-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002009
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002009
    reference: chr 11
allele count: 1
allele frequency: 4.789730817128078e-5
allele num: 20878
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-8C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-8C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1044C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1044C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1044C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1044C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1044C>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.75e1
  variant carriers: 0
hgvs: c.1426-8C>G
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

11-70002010-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002010
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002010
    reference: chr 11
allele count: 3
allele frequency: 1.435818895376663e-4
allele num: 20894
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1043C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-7C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-7C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1043C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1043C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1043C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1043C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4227
  bin: 9.75e1
  variant carriers: 3
hgvs: c.1426-7C>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

11-70002011-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002011
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002011
    reference: chr 11
allele count: 15
allele frequency: 7.17772035601493e-4
allele num: 20898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1042C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1042C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1042C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-6C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1042C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-6C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1042C>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2388
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4223
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1426-6C>G
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

11-70002012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002012
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002012
    reference: chr 11
allele count: 2664
allele frequency: 1.265558194774347e-1
allele num: 21050
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1426-5C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1041C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1041C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1041C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1041C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1041C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1426-5C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 2.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 2.5e0
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.5e0
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 9.75e1
  variant carriers: 701
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 2.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 130
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 134
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 6.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2020
  bin: 7.5e0
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 2.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 8.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 15
hgvs: c.1426-5C>T
num of homozygotes: 211
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD

11-70002021-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002021
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002021
    reference: chr 11
allele count: 1
allele frequency: 4.76462740613684e-5
allele num: 20988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1032G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1032G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1430G>A
  hgvsp: ENSP00000347454.5:p.Arg477His
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1032G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1032G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1430G>A
  hgvsp: ENSP00000444689.1:p.Arg477His
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1032G>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3247
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg477His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

11-70002023-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002023
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002023
    reference: chr 11
allele count: 2
allele frequency: 9.530162965786715e-5
allele num: 20986
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1432C>G
  hgvsp: ENSP00000347454.5:p.Arg478Gly
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1432C>G
  hgvsp: ENSP00000444689.1:p.Arg478Gly
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1030C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1030C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1030C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1030C>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1030C>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3247
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg478Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

11-70002023-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002023
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002023
    reference: chr 11
allele count: 1
allele frequency: 4.765081482893357e-5
allele num: 20986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1030C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1030C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1432C>T
  hgvsp: ENSP00000444689.1:p.Arg478Trp
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1030C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1030C>T
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1432C>T
  hgvsp: ENSP00000347454.5:p.Arg478Trp
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1030C>T
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3247
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg478Trp
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-70002024-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002024
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002024
    reference: chr 11
allele count: 1
allele frequency: 4.762358319839985e-5
allele num: 20998
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1433G>A
  hgvsp: ENSP00000347454.5:p.Arg478Gln
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1433G>A
  hgvsp: ENSP00000444689.1:p.Arg478Gln
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-1029G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-1029G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-1029G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-1029G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-1029G>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4361
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg478Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

11-70002087-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002087
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002087
    reference: chr 11
allele count: 3
allele frequency: 1.470588235294118e-4
allele num: 20400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1496T>G
  hgvsp: ENSP00000444689.1:p.Val499Gly
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-966T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-966T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-966T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-966T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1496T>G
  hgvsp: ENSP00000347454.5:p.Val499Gly
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-966T>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3206
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1208
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4121
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val499Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

11-70002093-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002093
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002093
    reference: chr 11
allele count: 1
allele frequency: 4.8534265191225e-5
allele num: 20604
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1502T>C
  hgvsp: ENSP00000347454.5:p.Leu501Ser
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1502T>C
  hgvsp: ENSP00000444689.1:p.Leu501Ser
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-960T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-960T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-960T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-960T>C
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-960T>C
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3246
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu501Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

11-70002099-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002099
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002099
    reference: chr 11
allele count: 7
allele frequency: 3.420975466718796e-4
allele num: 20462
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-954T>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-954T>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-954T>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-954T>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1503+5T>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1503+5T>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-954T>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1300
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3249
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1503+5T>A
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff

11-70002116-AGC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002116
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002114
    reference: chr 11
allele count: 1
allele frequency: 4.995004995004995e-5
allele num: 20020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-931_631-930delCG
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1503+28_1503+29delCG
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-931_1066-930delCG
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1503+28_1503+29delCG
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-931_1330-930delCG
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-931_157-930delCG
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-931_1066-930delCG
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: AGC
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

11-70002119-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002119
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002119
    reference: chr 11
allele count: 2
allele frequency: 1.00391526955125e-4
allele num: 19922
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-934G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-934G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-934G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-934G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1503+25G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1503+25G>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-934G>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1298
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2459
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
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: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-70002122-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002122
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002122
    reference: chr 11
allele count: 1
allele frequency: 5.04693650953871e-5
allele num: 19814
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1503+28C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1503+28C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-931C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-931C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-931C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-931C>A
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-931C>A
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2341
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

11-70002134-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002134
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002134
    reference: chr 11
allele count: 1
allele frequency: 5.076657528683115e-5
allele num: 19698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-919T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-919T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-919T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1503+40T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-919T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-919T>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1503+40T>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1497
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ

11-70002142-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70002142
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 70002142
    reference: chr 11
allele count: 1
allele frequency: 5.130309870716191e-5
allele num: 19492
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000319477
  ensembl transcript: ENST00000316296
  gene symbol: ANO1
  hgvsc: ENST00000316296.5:c.1330-911A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000381551
  ensembl transcript: ENST00000398543
  gene symbol: ANO1
  hgvsc: ENST00000398543.2:c.1066-911A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000444689
  ensembl transcript: ENST00000538023
  gene symbol: ANO1
  hgvsc: ENST00000538023.1:c.1503+48A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000432843
  ensembl transcript: ENST00000531349
  gene symbol: ANO1
  hgvsc: ENST00000531349.1:c.631-911A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000347454
  ensembl transcript: ENST00000355303
  gene symbol: ANO1
  hgvsc: ENST00000355303.5:c.1503+48A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435868
  ensembl transcript: ENST00000531300
  gene symbol: ANO1
  hgvsc: ENST00000531300.1:c.157-911A>G
  variant of: http://identifiers.org/hgnc/21625
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131620
  ensembl protein: ENSP00000435797
  ensembl transcript: ENST00000530676
  gene symbol: ANO1
  hgvsc: ENST00000530676.1:c.1066-911A>G
  variant of: http://identifiers.org/hgnc/21625
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22499
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 904
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4428
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.574002574002574e-4
allele num: 7770
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 4.385964912280702e-3
allele num: 228
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.11e-1

DP
type: SiteQuality
SIO_000300: 3.07637e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.556e0

FS
type: SiteQuality
SIO_000300: 3.3948e1

VQSLOD
type: SiteQuality
SIO_000300: -3.537e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.93e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.34e-1

MQ
type: SiteQuality
SIO_000300: 5.891e1

QD
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5310
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 930
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.63e0

DP
type: SiteQuality
SIO_000300: 3.04054e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.45e-2

QD
type: SiteQuality
SIO_000300: 1.215e1

GenotypeQuality
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7006
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.145922746781116e-3
allele num: 466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2974
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.459e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.47e0

FS
type: SiteQuality
SIO_000300: 8.7907e1

DP
type: SiteQuality
SIO_000300: 2.95415e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.064e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.531e0

MQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

GenotypeQuality
all individuals: 16929
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 261
bin: 4.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1271
bin: 6.25e1
variant carriers: 7

GenotypeQuality
all individuals: 365
bin: 7.25e1
variant carriers: 8

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 243
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 199
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 201
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 847
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 754
bin: 2.25e1
variant carriers: 10

Other
type: Population
allele count: 1
allele frequency: 7.936507936507936e-3
allele num: 126
num of homozygotes: 0

South Asian
type: Population
allele count: 23
allele frequency: 3.282900371110477e-3
allele num: 7006
num of homozygotes: 0

African
type: Population
allele count: 17
allele frequency: 3.648068669527897e-2
allele num: 466
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 2.857142857142857e-2
allele num: 140
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 13
allele frequency: 2.166666666666667e-1
allele num: 60
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 6.388702084734364e-3
allele num: 2974
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 1.149425287356322e-2
allele num: 174
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.459e0

MQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

DP
type: SiteQuality
SIO_000300: 2.95415e5

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.064e-1

FS
type: SiteQuality
SIO_000300: 8.7907e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

QD
type: SiteQuality
SIO_000300: 1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.531e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 391
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variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.185314685314685e-4
allele num: 4576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.865e1

DP
type: SiteQuality
SIO_000300: 3.12977e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.93e-2

FS
type: SiteQuality
SIO_000300: 1.177e0

VQSLOD
type: SiteQuality
SIO_000300: -2.54e0

QD
type: SiteQuality
SIO_000300: 5.31e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 220
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GenotypeQuality
all individuals: 14
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.185314685314685e-4
allele num: 4576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7804
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.177e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 3.12977e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.93e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.38e-1

MQ
type: SiteQuality
SIO_000300: 5.865e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.33e-1

QD
type: SiteQuality
SIO_000300: 5.31e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2226
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.18850306390429e-4
allele num: 13708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5524
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

FS
type: SiteQuality
SIO_000300: 3.42e0

DP
type: SiteQuality
SIO_000300: 1.485415e6

QD
type: SiteQuality
SIO_000300: 1.078e1

GenotypeQuality
all individuals: 2833
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13760
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.820078962210942e-4
allele num: 7092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53206
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8740
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.491898e6

QD
type: SiteQuality
SIO_000300: 1.43e1

FS
type: SiteQuality
SIO_000300: 7.089e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.171e0

VQSLOD
type: SiteQuality
SIO_000300: -9.733000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.885e1

GenotypeQuality
all individuals: 6470
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5610
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variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.872518912441016e-5
allele num: 53404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13788
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8792
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7104
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

DP
type: SiteQuality
SIO_000300: 1.521605e6

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.101e0

QD
type: SiteQuality
SIO_000300: 9.859999999999999e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13826
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7136
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.550819e6

MQ
type: SiteQuality
SIO_000300: 5.662e1

FS
type: SiteQuality
SIO_000300: 1.305e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.086e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.168e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.395355716609969e-5
allele num: 54088
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7166
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.456e0

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.580125e6

FS
type: SiteQuality
SIO_000300: 1.29905e2

QD
type: SiteQuality
SIO_000300: 3.4e0

MQRankSum
type: SiteQuality
SIO_000300: -9.03e-1

MQ
type: SiteQuality
SIO_000300: 5.072e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 2021
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variant carriers: 1

GenotypeQuality
all individuals: 776
bin: 7.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9078
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 11
allele frequency: 2.016350771712432e-4
allele num: 54554
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.8013e1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9118
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.654169407293722e-5
allele num: 54732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5622
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 13970
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.883e1

FS
type: SiteQuality
SIO_000300: 1.40298e2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.7e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.488e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.023e0

VQSLOD
type: SiteQuality
SIO_000300: -9.167e1

GenotypeQuality
all individuals: 988
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
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GenotypeQuality
all individuals: 312
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3433
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54882
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.19703136222169e-4
allele num: 8354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13994
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5646
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

QD
type: SiteQuality
SIO_000300: 1.59e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.503e0

DP
type: SiteQuality
SIO_000300: 1.615405e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

MQRankSum
type: SiteQuality
SIO_000300: -4.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e-1

GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9462
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9754
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7448
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.359603586597452e-4
allele num: 8476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56158
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5748
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 1.658029e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.21e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

QD
type: SiteQuality
SIO_000300: 1.337e1

GenotypeQuality
all individuals: 905
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23729
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variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56356
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.335826876836762e-4
allele num: 7486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14174
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

DP
type: SiteQuality
SIO_000300: 1.663554e6

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

FS
type: SiteQuality
SIO_000300: 6.853e0

MQ
type: SiteQuality
SIO_000300: 5.795e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.09e-1

QD
type: SiteQuality
SIO_000300: 1.072e1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2513
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5884
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7714
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58128
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.02757502027575e-4
allele num: 9864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.852e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.936e0

VQSLOD
type: SiteQuality
SIO_000300: -1.392e0

MQ
type: SiteQuality
SIO_000300: 5.739e1

FS
type: SiteQuality
SIO_000300: 4.058e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.708522e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

GenotypeQuality
all individuals: 75
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3046
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9464
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.679091947075022e-5
allele num: 59556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.725247e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.593e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

VQSLOD
type: SiteQuality
SIO_000300: -3.835e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.44e0

MQ
type: SiteQuality
SIO_000300: 5.838e1

QD
type: SiteQuality
SIO_000300: 6.1e0

GenotypeQuality
all individuals: 2538
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
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variant carriers: 0

GenotypeQuality
all individuals: 2507
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3196
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
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variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6008
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14614
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.13947128532361e-4
allele num: 8776
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 5.707e1

DP
type: SiteQuality
SIO_000300: 1.722945e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

VQSLOD
type: SiteQuality
SIO_000300: 5.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.77e-1

GenotypeQuality
all individuals: 651
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 7.5e0
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GenotypeQuality
all individuals: 24930
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 895
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variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 949
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variant carriers: 0

GenotypeQuality
all individuals: 408
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variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2489
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14668
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6018
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7926
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.136363636363636e-4
allele num: 8800
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.746e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.05e-1

DP
type: SiteQuality
SIO_000300: 1.720131e6

FS
type: SiteQuality
SIO_000300: 3.674e0

QD
type: SiteQuality
SIO_000300: 1.329e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

VQSLOD
type: SiteQuality
SIO_000300: -1.501e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeQuality
all individuals: 232
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 4.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 7.75e1
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GenotypeQuality
all individuals: 9707
bin: 9.75e1
variant carriers: 279

GenotypeQuality
all individuals: 406
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 291
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variant carriers: 3

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 24708
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 158
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.790483649892304e-5
allele num: 10214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.013368983957219e-5
allele num: 59840
num of homozygotes: 0

South Asian
type: Population
allele count: 17
allele frequency: 1.158038147138965e-3
allele num: 14680
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8798
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.5e-3
allele num: 800
num of homozygotes: 0

East Asian
type: Population
allele count: 286
allele frequency: 3.591160220994475e-2
allele num: 7964
num of homozygotes: 8

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6028
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.147e1

MQRankSum
type: SiteQuality
SIO_000300: 4.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

DP
type: SiteQuality
SIO_000300: 1.722308e6

FS
type: SiteQuality
SIO_000300: 1.106e0

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.17e-2

MQ
type: SiteQuality
SIO_000300: 5.854e1

GenotypeQuality
all individuals: 23219
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 4.75e1
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GenotypeQuality
all individuals: 9468
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GenotypeQuality
all individuals: 107
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8539
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2447
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59994
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7974
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14696
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.135589370883489e-4
allele num: 8806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.77e-1

DP
type: SiteQuality
SIO_000300: 1.712959e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -9.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.131e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.96e-1

MQ
type: SiteQuality
SIO_000300: 5.77e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.35e-1

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2457
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8552
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
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GenotypeQuality
all individuals: 775
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GenotypeQuality
all individuals: 893
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GenotypeQuality
all individuals: 148
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GenotypeQuality
all individuals: 295
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variant carriers: 0

GenotypeQuality
all individuals: 9471
bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60052
num of homozygotes: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 5.01002004008016e-4
allele num: 7984
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8810
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6044
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e-1

FS
type: SiteQuality
SIO_000300: 6.392e0

MQ
type: SiteQuality
SIO_000300: 5.843e1

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

DP
type: SiteQuality
SIO_000300: 1.713441e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

QD
type: SiteQuality
SIO_000300: 1.265e1

VQSLOD
type: SiteQuality
SIO_000300: -1.467e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.43e-1

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8624
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6050
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7984
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8812
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.498102403622079e-4
allele num: 60076
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.117e0

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.695304e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQ
type: SiteQuality
SIO_000300: 5.863e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.44e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 5648
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 407
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59942
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6066
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.812917291184085e-5
allele num: 14678
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 1.672547e6

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 1.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e-1

QD
type: SiteQuality
SIO_000300: 1.12e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

GenotypeQuality
all individuals: 14702
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 4.25e1
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: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2668
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9122
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3172
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3130
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.37e-2

DP
type: SiteQuality
SIO_000300: 8.10547e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.82e0

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

GenotypeQuality
all individuals: 862
bin: 5.75e1
variant carriers: 858

GenotypeQuality
all individuals: 864
bin: 8.25e1
variant carriers: 787

GenotypeQuality
all individuals: 7097
bin: 2.25e1
variant carriers: 5211

GenotypeQuality
all individuals: 869
bin: 6.75e1
variant carriers: 714

GenotypeQuality
all individuals: 678
bin: 7.75e1
variant carriers: 606

GenotypeQuality
all individuals: 1362
bin: 9.25e1
variant carriers: 1311

GenotypeQuality
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bin: 3.75e1
variant carriers: 2660

GenotypeQuality
all individuals: 481
bin: 7.25e1
variant carriers: 397

GenotypeQuality
all individuals: 947
bin: 8.75e1
variant carriers: 912

GenotypeQuality
all individuals: 17908
bin: 9.75e1
variant carriers: 17643

Latino
type: Population
allele count: 2710
allele frequency: 6.934493346980553e-1
allele num: 3908
num of homozygotes: 870

Other
type: Population
allele count: 365
allele frequency: 7.213438735177866e-1
allele num: 506
num of homozygotes: 130

South Asian
type: Population
allele count: 6326
allele frequency: 6.432784218019117e-1
allele num: 9834
num of homozygotes: 2041

European (Non-Finnish)
type: Population
allele count: 23937
allele frequency: 7.210374118922827e-1
allele num: 33198
num of homozygotes: 8374

African
type: Population
allele count: 3646
allele frequency: 6.855960887551711e-1
allele num: 5318
num of homozygotes: 1227

East Asian
type: Population
allele count: 3222
allele frequency: 7.862371888726208e-1
allele num: 4098
num of homozygotes: 1252

European (Finnish)
type: Population
allele count: 2635
allele frequency: 7.090958019375673e-1
allele num: 3716
num of homozygotes: 901

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.045e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 9.06303e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

QD
type: SiteQuality
SIO_000300: 2.738e1

GenotypeQuality
all individuals: 4319
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 834
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 767
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variant carriers: 0

GenotypeQuality
all individuals: 5355
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5258
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.039284971939306e-4
allele num: 9622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32502
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.05392e5

MQRankSum
type: SiteQuality
SIO_000300: 6.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.36e-1

QD
type: SiteQuality
SIO_000300: 8.48e0

GenotypeQuality
all individuals: 436
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3014
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21954
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
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variant carriers: 0

GenotypeQuality
all individuals: 770
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variant carriers: 0

GenotypeQuality
all individuals: 3584
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 855
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variant carriers: 0

GenotypeQuality
all individuals: 3134
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variant carriers: 0

GenotypeQuality
all individuals: 4865
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1100
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3962
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 1.21654501216545e-3
allele num: 4110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5312
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32808
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-2

QD
type: SiteQuality
SIO_000300: 1.003e1

VQSLOD
type: SiteQuality
SIO_000300: -3.067e-1

FS
type: SiteQuality
SIO_000300: 9.146000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.933e0

DP
type: SiteQuality
SIO_000300: 9.21965e5

GenotypeQuality
all individuals: 4319
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 783
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variant carriers: 0

GenotypeQuality
all individuals: 22376
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variant carriers: 0

GenotypeQuality
all individuals: 3786
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 316
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variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32978
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5324
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.030715316429602e-4
allele num: 9702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3986
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.157e0

VQSLOD
type: SiteQuality
SIO_000300: -5.865e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.466e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.375e0

QD
type: SiteQuality
SIO_000300: 1.196e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.51e-1

DP
type: SiteQuality
SIO_000300: 9.24803e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 242
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 4574
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6956
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3728
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4152
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

QD
type: SiteQuality
SIO_000300: 3.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

FS
type: SiteQuality
SIO_000300: 7.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.302e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.335e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.70252e5

GenotypeQuality
all individuals: 2944
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7153
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1243
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variant carriers: 0

GenotypeQuality
all individuals: 4052
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 796
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variant carriers: 0

GenotypeQuality
all individuals: 4516
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
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variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3758
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.876476464711759e-5
allele num: 34034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9852
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.08e-1

MQ
type: SiteQuality
SIO_000300: 5.836e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

DP
type: SiteQuality
SIO_000300: 9.73458e5

QD
type: SiteQuality
SIO_000300: 1.018e1

VQSLOD
type: SiteQuality
SIO_000300: -1.717e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-3

FS
type: SiteQuality
SIO_000300: 8.137e0

MQRankSum
type: SiteQuality
SIO_000300: 5.85e-1

GenotypeQuality
all individuals: 8774
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4077
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 8.75e1
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GenotypeQuality
all individuals: 644
bin: 9.25e1
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GenotypeQuality
all individuals: 1721
bin: 3.75e1
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GenotypeQuality
all individuals: 1272
bin: 6.75e1
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GenotypeQuality
all individuals: 799
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variant carriers: 0

GenotypeQuality
all individuals: 864
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GenotypeQuality
all individuals: 26804
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GenotypeQuality
all individuals: 438
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variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34824
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.224199288256228e-4
allele num: 4496
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3842
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

FS
type: SiteQuality
SIO_000300: 3.483e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

DP
type: SiteQuality
SIO_000300: 9.95494e5

QD
type: SiteQuality
SIO_000300: 1.231e1

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: 2.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5788
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.8833761612967e-5
allele num: 10118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3942
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4570
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 36102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4682
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.025419e6

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-1

QD
type: SiteQuality
SIO_000300: 1.234e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

FS
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SIO_000300: 1.845e0

MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.589e0

VQSLOD
type: SiteQuality
SIO_000300: 5.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3980
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4760
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4682
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5856
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South Asian
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allele count: 5
allele frequency: 4.906771344455348e-4
allele num: 10190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36614
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.299e0

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -7.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

FS
type: SiteQuality
SIO_000300: 6.268e0

QD
type: SiteQuality
SIO_000300: 1.168e1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.037452e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 39510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5172
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.869857890800299e-4
allele num: 5348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4180
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 3.235198964736332e-4
allele num: 6182
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 9.549274255156608e-5
allele num: 10472
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

QD
type: SiteQuality
SIO_000300: 1.025e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

DP
type: SiteQuality
SIO_000300: 1.088922e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e-1

GenotypeQuality
all individuals: 2564
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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
all individuals: 808
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4240
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 576
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.481635894381576e-5
allele num: 40296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5296
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.652e0

FS
type: SiteQuality
SIO_000300: 4.331e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -5.425e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

QD
type: SiteQuality
SIO_000300: 8.960000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.897e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 1.097325e6

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: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10560
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.590330788804071e-4
allele num: 6288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.481635894381576e-5
allele num: 40296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 576
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

MQ
type: SiteQuality
SIO_000300: 5.897e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.76e-1

FS
type: SiteQuality
SIO_000300: 4.331e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.097325e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 8.960000000000001e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 576
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5400
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 8.732099196646874e-4
allele num: 5726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41042
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4266
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.597e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.892e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

DP
type: SiteQuality
SIO_000300: 1.103726e6

QD
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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5506
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.399002015161693e-5
allele num: 41684
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 5838
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele num: 586
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African
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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QD
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MQ
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.22e-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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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4296
num of homozygotes: 0

Latino
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South Asian
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African
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.43261652233142e-5
allele num: 41108
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East Asian
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Other
type: Population
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.87e-1

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

European (Non-Finnish)
type: Population
allele count: 2
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allele num: 41060
num of homozygotes: 0

Latino
type: Population
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allele num: 5760
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.583280557314756e-4
allele num: 6316
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East Asian
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
type: Population
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VQSLOD
type: SiteQuality
SIO_000300: 4.9e-1

BaseQRankSum
type: SiteQuality
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.020079e6

FS
type: SiteQuality
SIO_000300: 7.767e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

GenotypeQuality
all individuals: 307
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1201
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4885
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 790
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19671
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4167
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.594896331738437e-4
allele num: 6270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4226
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10540
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.067e1

DP
type: SiteQuality
SIO_000300: 1.013161e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.336e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 504
bin: 7.25e1
variant carriers: 417

GenotypeQuality
all individuals: 964
bin: 6.75e1
variant carriers: 807

GenotypeQuality
all individuals: 1474
bin: 7.5e0
variant carriers: 593

GenotypeQuality
all individuals: 2565
bin: 2.5e0
variant carriers: 233

GenotypeQuality
all individuals: 637
bin: 7.75e1
variant carriers: 554

GenotypeQuality
all individuals: 800
bin: 8.75e1
variant carriers: 764

GenotypeQuality
all individuals: 1553
bin: 4.25e1
variant carriers: 1538

GenotypeQuality
all individuals: 3429
bin: 3.75e1
variant carriers: 3350

GenotypeQuality
all individuals: 724
bin: 8.25e1
variant carriers: 645

GenotypeQuality
all individuals: 23128
bin: 9.75e1
variant carriers: 22858

African
type: Population
allele count: 4813
allele frequency: 6.959224985540775e-1
allele num: 6916
num of homozygotes: 1619

East Asian
type: Population
allele count: 4687
allele frequency: 7.775381552753815e-1
allele num: 6028
num of homozygotes: 1786

South Asian
type: Population
allele count: 7224
allele frequency: 6.301465457083043e-1
allele num: 11464
num of homozygotes: 2257

Latino
type: Population
allele count: 4529
allele frequency: 6.935681470137826e-1
allele num: 6530
num of homozygotes: 1434

European (Finnish)
type: Population
allele count: 3319
allele frequency: 7.067717206132879e-1
allele num: 4696
num of homozygotes: 1126

European (Non-Finnish)
type: Population
allele count: 32542
allele frequency: 7.190330991205974e-1
allele num: 45258
num of homozygotes: 11246

Other
type: Population
allele count: 458
allele frequency: 7.246835443037974e-1
allele num: 632
num of homozygotes: 163

BaseQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.87e-2

DP
type: SiteQuality
SIO_000300: 1.17456e6

QD
type: SiteQuality
SIO_000300: 2.544e1

FS
type: SiteQuality
SIO_000300: 6.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.39e0

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

GenotypeQuality
all individuals: 293
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2775
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1164
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19626
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2926
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2688
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.788739865120861e-5
allele num: 26394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3064
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9032
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.87e-1

MQ
type: SiteQuality
SIO_000300: 5.7e1

FS
type: SiteQuality
SIO_000300: 3.471e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.35e-2

QD
type: SiteQuality
SIO_000300: 1.044e1

VQSLOD
type: SiteQuality
SIO_000300: -1.021e0

MQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

DP
type: SiteQuality
SIO_000300: 7.98442e5

GenotypeQuality
all individuals: 251
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2753
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2576
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3199
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2920
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.226179875333927e-4
allele num: 4492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3086
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8914
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.44e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.243000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 2.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.89091e5

QD
type: SiteQuality
SIO_000300: 2.591e1

GenotypeQuality
all individuals: 506
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 5958
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3207
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 130
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 352
bin: 5.25e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 3.180212014134276e-3
allele num: 2830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24892
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3030
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8860
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.48e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.179e1

FS
type: SiteQuality
SIO_000300: 5.579e0

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.85433e5

GenotypeQuality
all individuals: 197
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5910
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 423
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2136
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.345215759849906e-4
allele num: 8528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7842
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -7.871e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.49e-1

DP
type: SiteQuality
SIO_000300: 4.62081e5

MQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.14e-2

FS
type: SiteQuality
SIO_000300: 6.842e0

QD
type: SiteQuality
SIO_000300: 1.777e1

GenotypeQuality
all individuals: 424
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5909
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 168
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.276161306789178e-4
allele num: 7836
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.172058134083451e-4
allele num: 8532
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.58e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.62409e5

QD
type: SiteQuality
SIO_000300: 1.675e1

VQSLOD
type: SiteQuality
SIO_000300: -1.136e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

FS
type: SiteQuality
SIO_000300: 1.1809e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 479
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.276161306789178e-4
allele num: 7836
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.27e-1

DP
type: SiteQuality
SIO_000300: 4.62409e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

FS
type: SiteQuality
SIO_000300: 1.1809e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.58e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.136e0

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.675e1

GenotypeQuality
all individuals: 1141
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5936
bin: 9.75e1
variant carriers: 31

GenotypeQuality
all individuals: 186
bin: 1.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

East Asian
type: Population
allele count: 31
allele frequency: 5.065359477124183e-2
allele num: 612
num of homozygotes: 2

Other
type: Population
allele count: 1
allele frequency: 4.716981132075472e-3
allele num: 212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.340276152586005e-4
allele num: 8546
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.824e0

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.99e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.04e-2

DP
type: SiteQuality
SIO_000300: 4.6436e5

QD
type: SiteQuality
SIO_000300: 1.387e1

GenotypeQuality
all individuals: 679
bin: 6.25e1
variant carriers: 83

GenotypeQuality
all individuals: 687
bin: 2.5e0
variant carriers: 9

GenotypeQuality
all individuals: 93
bin: 8.75e1
variant carriers: 78

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 65

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 141

GenotypeQuality
all individuals: 151
bin: 8.25e1
variant carriers: 119

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 90

GenotypeQuality
all individuals: 8462
bin: 9.75e1
variant carriers: 8202

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 64

GenotypeQuality
all individuals: 111
bin: 7.25e1
variant carriers: 66

European (Non-Finnish)
type: Population
allele count: 5963
allele frequency: 6.924059451927543e-1
allele num: 8612
num of homozygotes: 2059

East Asian
type: Population
allele count: 446
allele frequency: 7.263843648208469e-1
allele num: 614
num of homozygotes: 163

South Asian
type: Population
allele count: 4858
allele frequency: 6.161846778285135e-1
allele num: 7884
num of homozygotes: 1534

Latino
type: Population
allele count: 264
allele frequency: 6.534653465346535e-1
allele num: 404
num of homozygotes: 84

Other
type: Population
allele count: 152
allele frequency: 7.102803738317757e-1
allele num: 214
num of homozygotes: 51

European (Finnish)
type: Population
allele count: 633
allele frequency: 7.080536912751678e-1
allele num: 894
num of homozygotes: 211

African
type: Population
allele count: 1415
allele frequency: 6.605975723622782e-1
allele num: 2142
num of homozygotes: 470

ClippingRankSum
type: SiteQuality
SIO_000300: -1.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e-1

DP
type: SiteQuality
SIO_000300: 5.50494e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.279e-1

QD
type: SiteQuality
SIO_000300: 2.227e1

VQSLOD
type: SiteQuality
SIO_000300: 6.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.734e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

MQ
type: SiteQuality
SIO_000300: 5.986e1

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3225
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2150
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.534854245880862e-4
allele num: 7890
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.124e0

DP
type: SiteQuality
SIO_000300: 4.68805e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.64e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e0

QD
type: SiteQuality
SIO_000300: 1.03e1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

GenotypeQuality
all individuals: 886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 238
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4208
bin: 9.75e1
variant carriers: 4

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

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

GenotypeQuality
all individuals: 278
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 6.973500697350069e-4
allele num: 8604
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 4.72057e5

FS
type: SiteQuality
SIO_000300: 6.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.56e-2

QD
type: SiteQuality
SIO_000300: 5.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
all individuals: 364
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 289
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.26806999746386e-4
allele num: 7886
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.664179104477612e-4
allele num: 2144
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.56e-2

DP
type: SiteQuality
SIO_000300: 4.72057e5

BaseQRankSum
type: SiteQuality
SIO_000300: -5.14e-1

QD
type: SiteQuality
SIO_000300: 5.23e0

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.09e-1

FS
type: SiteQuality
SIO_000300: 6.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

GenotypeQuality
all individuals: 902
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3469
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 936
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.800354699771979e-4
allele num: 7894
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.082e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.07e-2

MQ
type: SiteQuality
SIO_000300: 5.947e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.275e0

FS
type: SiteQuality
SIO_000300: 1.258e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

DP
type: SiteQuality
SIO_000300: 4.72968e5

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.68e-1

GenotypeQuality
all individuals: 119
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2446
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3469
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4225
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 936
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.651162790697675e-4
allele num: 2150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 4.72968e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.07e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.275e0

QD
type: SiteQuality
SIO_000300: 1.082e1

MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 1.258e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2150
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.801317790167258e-4
allele num: 7892
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.953e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.54e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.54e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.45e-1

FS
type: SiteQuality
SIO_000300: 7.396e0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e-1

QD
type: SiteQuality
SIO_000300: 1.42e1

DP
type: SiteQuality
SIO_000300: 4.72923e5

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 950
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.155001155001155e-3
allele num: 8658
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 6.335529650278763e-4
allele num: 7892
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.44e-2

DP
type: SiteQuality
SIO_000300: 4.73187e5

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.829e0

FS
type: SiteQuality
SIO_000300: 2.768e0

QD
type: SiteQuality
SIO_000300: 1.158e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

GenotypeQuality
all individuals: 85
bin: 2.75e1
variant carriers: 10

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 15

GenotypeQuality
all individuals: 336
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 186
bin: 9.25e1
variant carriers: 11

GenotypeQuality
all individuals: 4824
bin: 9.75e1
variant carriers: 2419

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 269
bin: 7.25e1
variant carriers: 10

GenotypeQuality
all individuals: 3386
bin: 6.25e1
variant carriers: 12

GenotypeQuality
all individuals: 240
bin: 8.25e1
variant carriers: 7

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

European (Non-Finnish)
type: Population
allele count: 1412
allele frequency: 1.625230202578269e-1
allele num: 8688
num of homozygotes: 118

European (Finnish)
type: Population
allele count: 237
allele frequency: 2.231638418079096e-1
allele num: 1062
num of homozygotes: 19

Latino
type: Population
allele count: 42
allele frequency: 1.029411764705882e-1
allele num: 408
num of homozygotes: 1

Other
type: Population
allele count: 27
allele frequency: 1.194690265486726e-1
allele num: 226
num of homozygotes: 1

South Asian
type: Population
allele count: 908
allele frequency: 1.150240689130986e-1
allele num: 7894
num of homozygotes: 71

African
type: Population
allele count: 38
allele frequency: 1.767441860465116e-2
allele num: 2150
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.88e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 5.34034e5

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

QD
type: SiteQuality
SIO_000300: 1.529e1

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4350
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 276
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 9.823182711198428e-4
allele num: 1018
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8686
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.63504e5

VQSLOD
type: SiteQuality
SIO_000300: -1.534e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.64e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.441e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.879999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

QD
type: SiteQuality
SIO_000300: 1.775e1

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1053
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4352
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 2.535496957403651e-4
allele num: 7888
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1014
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.91e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

FS
type: SiteQuality
SIO_000300: 1.3197e1

QD
type: SiteQuality
SIO_000300: 7.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.957e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

DP
type: SiteQuality
SIO_000300: 4.63292e5

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 7.5e0
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GenotypeQuality
all individuals: 1053
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 213
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.607717041800643e-3
allele num: 622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1014
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.957e0

DP
type: SiteQuality
SIO_000300: 4.63292e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.91e-2

FS
type: SiteQuality
SIO_000300: 1.3197e1

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

QD
type: SiteQuality
SIO_000300: 7.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2150
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.267748478701826e-4
allele num: 7888
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.72e-2

FS
type: SiteQuality
SIO_000300: 2.68e0

DP
type: SiteQuality
SIO_000300: 4.63315e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQRankSum
type: SiteQuality
SIO_000300: 8.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

QD
type: SiteQuality
SIO_000300: 9.15e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
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variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 3.532736693358455e-4
allele num: 8492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.7096e2

DP
type: SiteQuality
SIO_000300: 4.56757e5

VQSLOD
type: SiteQuality
SIO_000300: -3.314e2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e0

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.671e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.69e-2

QD
type: SiteQuality
SIO_000300: 1.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.32e0

GenotypeQuality
all individuals: 120
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 897
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variant carriers: 0

GenotypeQuality
all individuals: 10
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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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variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.439024390243902e-3
allele num: 410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7790
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.29e-2

MQ
type: SiteQuality
SIO_000300: 5.914e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.53e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.08e-1

DP
type: SiteQuality
SIO_000300: 4.55282e5

FS
type: SiteQuality
SIO_000300: 9.85e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.221e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.428e0

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

GenotypeQuality
all individuals: 76
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3934
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 296
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GenotypeQuality
all individuals: 353
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variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 9.050943884147918e-4
allele num: 7734
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.23e1

MQRankSum
type: SiteQuality
SIO_000300: -2.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.113e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.49e-1

DP
type: SiteQuality
SIO_000300: 4.5143e5

FS
type: SiteQuality
SIO_000300: 6.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.28e-2

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.192463629859289e-4
allele num: 8386
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.85e-1

QD
type: SiteQuality
SIO_000300: 1.686e1

DP
type: SiteQuality
SIO_000300: 4.26093e5

MQRankSum
type: SiteQuality
SIO_000300: 2.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.27e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-1

FS
type: SiteQuality
SIO_000300: 4.705e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

MQ
type: SiteQuality
SIO_000300: 5.866e1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 128
bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

African
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allele count: 2
allele frequency: 9.319664492078285e-4
allele num: 2146
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7532
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.091e0

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e0

DP
type: SiteQuality
SIO_000300: 4.21204e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.27e-2

FS
type: SiteQuality
SIO_000300: 5.76e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 1.572e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.336541031809677e-4
allele num: 7482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.38e-1

DP
type: SiteQuality
SIO_000300: 4.18123e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.33e-1

FS
type: SiteQuality
SIO_000300: 3.163e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.27e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.82e-1

QD
type: SiteQuality
SIO_000300: 1.229e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8296
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 576
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.342281879194631e-4
allele num: 7450
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2144
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.157e0

QD
type: SiteQuality
SIO_000300: 3.76e0

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 6.0e1