4-114120310-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114120310
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114120310
    reference: chr 4
allele count: 1
allele frequency: 8.469551960701279e-6
allele num: 118070
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.321+45A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.429+45A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.384+45A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.384+45A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.429+45A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.-22+45A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.321+45A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.321+45A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.384+45A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11794
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11793
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4181
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2470
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

4-114153267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153267
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153267
    reference: chr 4
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.385-50C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.-21-50C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.385-50C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.430-50C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.322-50C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.322-50C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.322-50C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.430-50C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.385-50C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9839
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12025
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

4-114153269-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153269
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153269
    reference: chr 4
allele count: 1
allele frequency: 8.287475966319697e-6
allele num: 120664
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.322-48C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.-21-48C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.385-48C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.322-48C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.430-48C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.385-48C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.385-48C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.430-48C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.322-48C>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2039
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25164
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7912
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3035
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

4-114153275-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153275
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153275
    reference: chr 4
allele count: 1
allele frequency: 8.284180528862085e-6
allele num: 120712
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.430-42T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.322-42T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.-21-42T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.385-42T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.385-42T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.385-42T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.322-42T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.322-42T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.430-42T>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7914
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27206
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1989
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

4-114153275-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153275
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153275
    reference: chr 4
allele count: 1
allele frequency: 8.284180528862085e-6
allele num: 120712
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.-21-42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.385-42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.385-42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.322-42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.322-42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.430-42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.385-42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.322-42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.430-42T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9854
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7914
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

4-114153280-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153280
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153280
    reference: chr 4
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.322-37A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.385-37A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.322-37A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.430-37A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.385-37A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.-21-37A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.430-37A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.385-37A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.322-37A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2606
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2910
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

4-114153281-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153281
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153281
    reference: chr 4
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.322-36T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.322-36T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.430-36T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.385-36T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.430-36T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.385-36T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.322-36T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.-21-36T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.385-36T>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

4-114153290-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153290
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153290
    reference: chr 4
allele count: 10
allele frequency: 8.267332462507647e-5
allele num: 120958
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.322-27G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.385-27G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.430-27G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.430-27G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.385-27G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.385-27G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.322-27G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.-21-27G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.322-27G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20563
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9979
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2600
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

4-114153292-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153292
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153292
    reference: chr 4
allele count: 1
allele frequency: 8.263370132874991e-6
allele num: 121016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.-21-25G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.385-25G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.385-25G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.322-25G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.430-25G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.322-25G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.322-25G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.385-25G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.430-25G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ

4-114153311-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153311
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153311
    reference: chr 4
allele count: 9
allele frequency: 7.418397626112759e-5
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.322-6C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.430-6C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.-21-6C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.322-6C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.385-6C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.385-6C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.430-6C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.385-6C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.322-6C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
hgvs: c.385-6C>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

4-114153328-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153328
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153328
    reference: chr 4
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.333T>C
  hgvsp: ENST00000503271.1:c.333T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.-10T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.441T>C
  hgvsp: ENST00000508613.1:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.396T>C
  hgvsp: ENST00000394537.3:c.396T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.333T>C
  hgvsp: ENST00000503423.1:c.333T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.441T>C
  hgvsp: ENST00000504454.1:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.396T>C
  hgvsp: ENST00000264366.6:c.396T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.333T>C
  hgvsp: ENST00000506722.1:c.333T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.396T>C
  hgvsp: ENST00000357077.4:c.396T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2875
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2593
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11991
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Thr132Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

4-114153337-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153337
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153337
    reference: chr 4
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.342C>T
  hgvsp: ENST00000503423.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.450C>T
  hgvsp: ENST00000504454.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.405C>T
  hgvsp: ENST00000394537.3:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.342C>T
  hgvsp: ENST00000503271.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.450C>T
  hgvsp: ENST00000508613.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.342C>T
  hgvsp: ENST00000506722.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.405C>T
  hgvsp: ENST00000264366.6:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.-1C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.405C>T
  hgvsp: ENST00000357077.4:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8012
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2875
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr135Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-114153345-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153345
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153345
    reference: chr 4
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.413C>T
  hgvsp: ENSP00000378044.3:p.Ala138Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.350C>T
  hgvsp: ENSP00000423799.1:p.Ala117Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.458C>T
  hgvsp: ENSP00000424722.1:p.Ala153Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.350C>T
  hgvsp: ENSP00000421011.1:p.Ala117Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.413C>T
  hgvsp: ENSP00000264366.6:p.Ala138Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.8C>T
  hgvsp: ENSP00000421059.1:p.Ala3Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.458C>T
  hgvsp: ENSP00000422900.1:p.Ala153Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.350C>T
  hgvsp: ENSP00000421067.1:p.Ala117Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.413C>T
  hgvsp: ENSP00000349588.4:p.Ala138Val
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala138Val
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

4-114153370-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153370
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153370
    reference: chr 4
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.375A>G
  hgvsp: ENST00000506722.1:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.483A>G
  hgvsp: ENST00000508613.1:c.483A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.438A>G
  hgvsp: ENST00000357077.4:c.438A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.33A>G
  hgvsp: ENST00000515034.1:c.33A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.438A>G
  hgvsp: ENST00000264366.6:c.438A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.375A>G
  hgvsp: ENST00000503423.1:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.483A>G
  hgvsp: ENST00000504454.1:c.483A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.438A>G
  hgvsp: ENST00000394537.3:c.438A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.375A>G
  hgvsp: ENST00000503271.1:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8010
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val146Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

4-114153373-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153373
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153373
    reference: chr 4
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.36A>T
  hgvsp: ENSP00000421059.1:p.Lys12Asn
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.486A>T
  hgvsp: ENSP00000422900.1:p.Lys162Asn
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.441A>T
  hgvsp: ENSP00000349588.4:p.Lys147Asn
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.378A>T
  hgvsp: ENSP00000421067.1:p.Lys126Asn
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.441A>T
  hgvsp: ENSP00000264366.6:p.Lys147Asn
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.378A>T
  hgvsp: ENSP00000423799.1:p.Lys126Asn
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.441A>T
  hgvsp: ENSP00000378044.3:p.Lys147Asn
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.486A>T
  hgvsp: ENSP00000424722.1:p.Lys162Asn
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.378A>T
  hgvsp: ENSP00000421011.1:p.Lys126Asn
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31263
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys147Asn
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

4-114153393-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153393
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153393
    reference: chr 4
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.56C>G
  hgvsp: ENSP00000421059.1:p.Ala19Gly
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.506C>G
  hgvsp: ENSP00000424722.1:p.Ala169Gly
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.461C>G
  hgvsp: ENSP00000264366.6:p.Ala154Gly
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.398C>G
  hgvsp: ENSP00000421067.1:p.Ala133Gly
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.398C>G
  hgvsp: ENSP00000421011.1:p.Ala133Gly
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.461C>G
  hgvsp: ENSP00000349588.4:p.Ala154Gly
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.398C>G
  hgvsp: ENSP00000423799.1:p.Ala133Gly
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.506C>G
  hgvsp: ENSP00000422900.1:p.Ala169Gly
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.461C>G
  hgvsp: ENSP00000378044.3:p.Ala154Gly
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala154Gly
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

4-114153407-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153407
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153407
    reference: chr 4
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.520G>C
  hgvsp: ENSP00000422900.1:p.Ala174Pro
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.412G>C
  hgvsp: ENSP00000423799.1:p.Ala138Pro
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.475G>C
  hgvsp: ENSP00000264366.6:p.Ala159Pro
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.475G>C
  hgvsp: ENSP00000349588.4:p.Ala159Pro
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.475G>C
  hgvsp: ENSP00000378044.3:p.Ala159Pro
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.70G>C
  hgvsp: ENSP00000421059.1:p.Ala24Pro
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.412G>C
  hgvsp: ENSP00000421067.1:p.Ala138Pro
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.520G>C
  hgvsp: ENSP00000424722.1:p.Ala174Pro
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.412G>C
  hgvsp: ENSP00000421011.1:p.Ala138Pro
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7943
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala159Pro
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

4-114153410-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153410
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153410
    reference: chr 4
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.415A>G
  hgvsp: ENSP00000423799.1:p.Thr139Ala
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.478A>G
  hgvsp: ENSP00000349588.4:p.Thr160Ala
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.478A>G
  hgvsp: ENSP00000378044.3:p.Thr160Ala
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.415A>G
  hgvsp: ENSP00000421011.1:p.Thr139Ala
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.478A>G
  hgvsp: ENSP00000264366.6:p.Thr160Ala
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.523A>G
  hgvsp: ENSP00000424722.1:p.Thr175Ala
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.73A>G
  hgvsp: ENSP00000421059.1:p.Thr25Ala
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.523A>G
  hgvsp: ENSP00000422900.1:p.Thr175Ala
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.415A>G
  hgvsp: ENSP00000421067.1:p.Thr139Ala
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2573
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr160Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-114153416-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153416
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153416
    reference: chr 4
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.483+1G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.483+1G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.420+1G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.528+1G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.528+1G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.420+1G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.420+1G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.483+1G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.78+1G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: c.483+1G>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

4-114153421-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153421
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153421
    reference: chr 4
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.420+6A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.528+6A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.483+6A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.78+6A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.483+6A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.420+6A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.528+6A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.420+6A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.483+6A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11985
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: c.483+6A>G
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

4-114153423-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153423
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153423
    reference: chr 4
allele count: 2
allele frequency: 1.653685237551884e-5
allele num: 120942
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.420+8T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.78+8T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.420+8T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.483+8T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.528+8T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.420+8T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.483+8T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.528+8T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.483+8T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10017
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30136
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11986
  bin: 9.75e1
  variant carriers: 2
hgvs: c.483+8T>C
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/4-114153435-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153435
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153435
    reference: chr 4
allele count: 1
allele frequency: 8.315316813570598e-6
allele num: 120260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.528+20A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.420+20A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.483+20A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.483+20A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.528+20A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.420+20A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.483+20A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.78+20A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.420+20A>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2738
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11978
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-114153446-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153446
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153446
    reference: chr 4
allele count: 5
allele frequency: 4.178994701034719e-5
allele num: 119646
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.483+31C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.483+31C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.528+31C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.483+31C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.420+31C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.420+31C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.78+31C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.420+31C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.528+31C>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2634
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11968
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ

4-114153452-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114153452
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114153452
    reference: chr 4
allele count: 3
allele frequency: 2.514879704920781e-5
allele num: 119290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.420+37T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.420+37T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.483+37T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.78+37T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.528+37T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.528+37T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.483+37T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.483+37T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.420+37T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7853
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2113
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3610
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5882
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17916
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

4-114158096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158096
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158096
    reference: chr 4
allele count: 1
allele frequency: 8.343345347750633e-6
allele num: 119856
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.421-47A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.529-47A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.529-47A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.79-47A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.484-47A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.484-47A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.421-47A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.421-47A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.484-47A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3865
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4314
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2339
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3593
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-114158107-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158107
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158107
    reference: chr 4
allele count: 1
allele frequency: 8.329307501374335e-6
allele num: 120058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.484-36A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.529-36A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.421-36A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.484-36A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.421-36A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.79-36A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.484-36A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.421-36A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.529-36A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

4-114158108-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158108
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158108
    reference: chr 4
allele count: 3
allele frequency: 2.498292833230626e-5
allele num: 120082
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.421-35T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.484-35T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.484-35T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.484-35T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.79-35T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.529-35T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.421-35T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.529-35T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.421-35T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4454
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

4-114158111-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158111
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158111
    reference: chr 4
allele count: 58
allele frequency: 4.827459923759426e-4
allele num: 120146
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.79-32T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.421-32T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.484-32T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.421-32T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.484-32T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.484-32T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.529-32T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.421-32T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.529-32T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10938
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10851
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24985
  bin: 9.75e1
  variant carriers: 58
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

4-114158111-TAACA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158111
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158107
    reference: chr 4
allele count: 1
allele frequency: 8.323206765102459e-6
allele num: 120146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.421-31_421-28delAACA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.484-31_484-28delAACA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.529-31_529-28delAACA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.529-31_529-28delAACA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.421-31_421-28delAACA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.421-31_421-28delAACA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.484-31_484-28delAACA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.484-31_484-28delAACA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.79-31_79-28delAACA
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5404
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: TAACA
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

4-114158125-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158125
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158125
    reference: chr 4
allele count: 2
allele frequency: 1.661709234118214e-5
allele num: 120358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.79-18T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.529-18T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.484-18T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.421-18T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.484-18T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.421-18T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.421-18T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.484-18T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.529-18T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

4-114158128-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158128
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158128
    reference: chr 4
allele count: 2
allele frequency: 1.661239949498306e-5
allele num: 120392
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.484-15C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.421-15C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.484-15C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.421-15C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.484-15C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.529-15C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.421-15C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.529-15C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.79-15C>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2925
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3678
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

4-114158139-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158139
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158139
    reference: chr 4
allele count: 1
allele frequency: 8.297515723792297e-6
allele num: 120518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.79-4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.421-4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.421-4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.421-4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.484-4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.484-4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.529-4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422900
  ensembl transcript: ENST00000508613
  gene symbol: ANK2
  hgvsc: ENST00000508613.1:c.529-4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.484-4C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11416
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4673
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: c.484-4C>T
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: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/4-114158172-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158172
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158172
    reference: chr 4
allele count: 1
allele frequency: 8.265009256810368e-6
allele num: 120992
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.450C>A
  hgvsp: ENST00000503423.1:c.450C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.108C>A
  hgvsp: ENST00000515034.1:c.108C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.450C>A
  hgvsp: ENST00000503271.1:c.450C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.513C>A
  hgvsp: ENST00000264366.6:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.513C>A
  hgvsp: ENST00000394537.3:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.450C>A
  hgvsp: ENST00000506722.1:c.450C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.558C>A
  hgvsp: ENST00000504454.1:c.558C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.513C>A
  hgvsp: ENST00000357077.4:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2931
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24965
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu171Leu
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: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-114158181-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158181
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158181
    reference: chr 4
allele count: 1
allele frequency: 8.260093834665961e-6
allele num: 121064
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.522A>G
  hgvsp: ENST00000394537.3:c.522A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.459A>G
  hgvsp: ENST00000503423.1:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.522A>G
  hgvsp: ENST00000357077.4:c.522A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.522A>G
  hgvsp: ENST00000264366.6:c.522A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.117A>G
  hgvsp: ENST00000515034.1:c.117A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.567A>G
  hgvsp: ENST00000504454.1:c.567A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.459A>G
  hgvsp: ENST00000503271.1:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.459A>G
  hgvsp: ENST00000506722.1:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4675
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly174Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

4-114158193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158193
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158193
    reference: chr 4
allele count: 11
allele frequency: 9.080252926317875e-5
allele num: 121142
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.579G>A
  hgvsp: ENST00000504454.1:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.471G>A
  hgvsp: ENST00000506722.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.129G>A
  hgvsp: ENST00000515034.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.534G>A
  hgvsp: ENST00000357077.4:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.471G>A
  hgvsp: ENST00000503423.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.471G>A
  hgvsp: ENST00000503271.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.534G>A
  hgvsp: ENST00000394537.3:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.534G>A
  hgvsp: ENST00000264366.6:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3678
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala178Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

4-114158206-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158206
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158206
    reference: chr 4
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.547T>C
  hgvsp: ENST00000394537.3:c.547T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.547T>C
  hgvsp: ENST00000357077.4:c.547T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.142T>C
  hgvsp: ENST00000515034.1:c.142T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.484T>C
  hgvsp: ENST00000506722.1:c.484T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.592T>C
  hgvsp: ENST00000504454.1:c.592T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.484T>C
  hgvsp: ENST00000503271.1:c.484T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.484T>C
  hgvsp: ENST00000503423.1:c.484T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.547T>C
  hgvsp: ENST00000264366.6:c.547T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu183Leu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-114158239-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158239
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158239
    reference: chr 4
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.625C>A
  hgvsp: ENSP00000424722.1:p.Pro209Thr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.517C>A
  hgvsp: ENSP00000421067.1:p.Pro173Thr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.580C>A
  hgvsp: ENSP00000264366.6:p.Pro194Thr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.175C>A
  hgvsp: ENSP00000421059.1:p.Pro59Thr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.517C>A
  hgvsp: ENSP00000423799.1:p.Pro173Thr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.580C>A
  hgvsp: ENSP00000378044.3:p.Pro194Thr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.517C>A
  hgvsp: ENSP00000421011.1:p.Pro173Thr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.580C>A
  hgvsp: ENSP00000349588.4:p.Pro194Thr
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11814
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro194Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

4-114158256-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158256
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158256
    reference: chr 4
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.534C>T
  hgvsp: ENST00000506722.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421059
  ensembl transcript: ENST00000515034
  gene symbol: ANK2
  hgvsc: ENST00000515034.1:c.192C>T
  hgvsp: ENST00000515034.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.534C>T
  hgvsp: ENST00000503271.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.597C>T
  hgvsp: ENST00000394537.3:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.534C>T
  hgvsp: ENST00000503423.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.642C>T
  hgvsp: ENST00000504454.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.597C>T
  hgvsp: ENST00000264366.6:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.597C>T
  hgvsp: ENST00000357077.4:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11098
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4678
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24967
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala199Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

4-114158274-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158274
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158274
    reference: chr 4
allele count: 8
allele frequency: 6.595870984763538e-5
allele num: 121288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.660C>T
  hgvsp: ENST00000504454.1:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.552C>T
  hgvsp: ENST00000506722.1:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.552C>T
  hgvsp: ENST00000503423.1:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.552C>T
  hgvsp: ENST00000503271.1:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.615C>T
  hgvsp: ENST00000394537.3:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.615C>T
  hgvsp: ENST00000264366.6:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.615C>T
  hgvsp: ENST00000357077.4:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2930
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4676
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5526
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr205Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

4-114158283-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158283
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158283
    reference: chr 4
allele count: 4
allele frequency: 3.298044259753966e-5
allele num: 121284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.669C>T
  hgvsp: ENST00000504454.1:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.561C>T
  hgvsp: ENST00000506722.1:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.561C>T
  hgvsp: ENST00000503423.1:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.624C>T
  hgvsp: ENST00000357077.4:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.624C>T
  hgvsp: ENST00000264366.6:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.624C>T
  hgvsp: ENST00000394537.3:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.561C>T
  hgvsp: ENST00000503271.1:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24968
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2929
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala208Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ

4-114158289-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158289
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158289
    reference: chr 4
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.567T>C
  hgvsp: ENST00000503271.1:c.567T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.675T>C
  hgvsp: ENST00000504454.1:c.675T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.567T>C
  hgvsp: ENST00000503423.1:c.567T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.630T>C
  hgvsp: ENST00000264366.6:c.630T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.567T>C
  hgvsp: ENST00000506722.1:c.567T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.630T>C
  hgvsp: ENST00000394537.3:c.630T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.630T>C
  hgvsp: ENST00000357077.4:c.630T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11094
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5522
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11839
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu210Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD

4-114158289-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158289
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158289
    reference: chr 4
allele count: 2
allele frequency: 1.649049323065253e-5
allele num: 121282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.567T>G
  hgvsp: ENST00000503271.1:c.567T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.567T>G
  hgvsp: ENST00000503423.1:c.567T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.675T>G
  hgvsp: ENST00000504454.1:c.675T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.630T>G
  hgvsp: ENST00000357077.4:c.630T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.630T>G
  hgvsp: ENST00000394537.3:c.630T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.630T>G
  hgvsp: ENST00000264366.6:c.630T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.567T>G
  hgvsp: ENST00000506722.1:c.567T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4673
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24966
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3678
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4474
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu210Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

4-114158304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158304
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158304
    reference: chr 4
allele count: 2
allele frequency: 1.649130908011478e-5
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.645C>T
  hgvsp: ENST00000264366.6:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.582C>T
  hgvsp: ENST00000503271.1:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.645C>T
  hgvsp: ENST00000394537.3:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.582C>T
  hgvsp: ENST00000506722.1:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.645C>T
  hgvsp: ENST00000357077.4:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.690C>T
  hgvsp: ENST00000504454.1:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.582C>T
  hgvsp: ENST00000503423.1:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5512
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2925
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4667
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3678
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp215Asp
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-114158316-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158316
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158316
    reference: chr 4
allele count: 2
allele frequency: 1.649402916144356e-5
allele num: 121256
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.657C>T
  hgvsp: ENST00000357077.4:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.657C>T
  hgvsp: ENST00000394537.3:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.702C>T
  hgvsp: ENST00000504454.1:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.594C>T
  hgvsp: ENST00000503423.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.657C>T
  hgvsp: ENST00000264366.6:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.594C>T
  hgvsp: ENST00000503271.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.594C>T
  hgvsp: ENST00000506722.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3678
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5506
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp219Asp
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

4-114158317-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158317
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158317
    reference: chr 4
allele count: 2
allele frequency: 1.649538953862396e-5
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.595G>A
  hgvsp: ENSP00000423799.1:p.Val199Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.658G>A
  hgvsp: ENSP00000264366.6:p.Val220Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.658G>A
  hgvsp: ENSP00000349588.4:p.Val220Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.595G>A
  hgvsp: ENSP00000421067.1:p.Val199Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.658G>A
  hgvsp: ENSP00000378044.3:p.Val220Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.703G>A
  hgvsp: ENSP00000424722.1:p.Val235Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.595G>A
  hgvsp: ENSP00000421011.1:p.Val199Ile
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11066
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3678
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4474
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11798
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val220Ile
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

4-114158321-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158321
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158321
    reference: chr 4
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.662A>G
  hgvsp: ENSP00000264366.6:p.Gln221Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.662A>G
  hgvsp: ENSP00000378044.3:p.Gln221Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.599A>G
  hgvsp: ENSP00000421067.1:p.Gln200Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.599A>G
  hgvsp: ENSP00000421011.1:p.Gln200Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.599A>G
  hgvsp: ENSP00000423799.1:p.Gln200Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.662A>G
  hgvsp: ENSP00000349588.4:p.Gln221Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.707A>G
  hgvsp: ENSP00000424722.1:p.Gln236Arg
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11054
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24969
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4473
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln221Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

4-114158331-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158331
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158331
    reference: chr 4
allele count: 16
allele frequency: 1.320110229204139e-4
allele num: 121202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.669+3A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.606+3A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.714+3A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.606+3A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.669+3A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.606+3A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.669+3A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3677
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24978
  bin: 9.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 11687
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: c.669+3A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-114158337-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158337
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158337
    reference: chr 4
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.606+9A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.669+9A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.669+9A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.714+9A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.669+9A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.606+9A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.606+9A>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11631
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5458
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24970
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4468
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

4-114158337-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158337
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158337
    reference: chr 4
allele count: 2
allele frequency: 1.650273945474949e-5
allele num: 121192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.669+9A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.669+9A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.669+9A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.606+9A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.714+9A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.606+9A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.606+9A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2913
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum

http://identifiers.org/exac.variant/4-114158342-AAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158342
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158340
    reference: chr 4
allele count: 2
allele frequency: 1.650546330835507e-5
allele num: 121172
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.669+18_669+19delCA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.669+18_669+19delCA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.606+18_606+19delCA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.669+18_669+19delCA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.606+18_606+19delCA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.606+18_606+19delCA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.714+18_714+19delCA
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5445
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24968
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3676
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: AAC
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

4-114158347-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158347
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158347
    reference: chr 4
allele count: 1
allele frequency: 8.253821519363466e-6
allele num: 121156
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.669+19A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.606+19A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.606+19A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.669+19A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.714+19A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.606+19A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.669+19A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24967
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11458
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

4-114158350-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158350
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158350
    reference: chr 4
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.669+22T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.669+22T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.606+22T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.606+22T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.669+22T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.714+22T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.606+22T>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10974
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4460
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24967
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4651
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3676
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

4-114158362-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158362
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158362
    reference: chr 4
allele count: 2
allele frequency: 1.651855033202286e-5
allele num: 121076
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.669+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.669+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.714+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.669+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.606+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.606+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.606+34C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4452
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5328
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2889
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4635
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10781
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

4-114158369-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158369
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158369
    reference: chr 4
allele count: 1
allele frequency: 8.263370132874991e-6
allele num: 121016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.714+41G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.669+41G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.606+41G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.606+41G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.669+41G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.606+41G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.669+41G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5272
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10119
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3672
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-114158380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158380
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158380
    reference: chr 4
allele count: 3
allele frequency: 2.483320364882539e-5
allele num: 120806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.606+52C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.669+52C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.669+52C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.606+52C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.606+52C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.669+52C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.714+52C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8163
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8264
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5839
  bin: 4.25e1
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genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7023
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
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genotype quality: GenotypeQuality
  all individuals: 4578
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-114158705-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158705
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158705
    reference: chr 4
allele count: 8
allele frequency: 6.59043727551323e-5
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.670-50T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.607-50T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.607-50T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.607-50T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.670-50T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.715-50T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.670-50T>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6037
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8140
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5874
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3813
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1996
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4047
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

4-114158706-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158706
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158706
    reference: chr 4
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.715-49T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.670-49T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.607-49T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.607-49T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.607-49T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.670-49T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.670-49T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7372
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5890
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34567
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

4-114158713-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158713
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158713
    reference: chr 4
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.670-42G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.670-42G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.607-42G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.607-42G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.607-42G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.715-42G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.670-42G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6038
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34559
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3999
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4033
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

4-114158714-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158714
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158714
    reference: chr 4
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.607-41T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.670-41T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.607-41T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.670-41T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.607-41T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.670-41T>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.715-41T>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6036
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6035
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4035
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2173
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-114158717-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158717
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158717
    reference: chr 4
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.607-38A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.670-38A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.670-38A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.607-38A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.607-38A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.670-38A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.715-38A>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2172
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

4-114158720-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158720
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158720
    reference: chr 4
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.607-35A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.607-35A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.670-35A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.670-35A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.607-35A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.670-35A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.715-35A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4728
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6037
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4013
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6079
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

4-114158725-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158725
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158725
    reference: chr 4
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.670-30C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.715-30C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.607-30C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.607-30C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.670-30C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.670-30C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.607-30C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4028
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4008
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6090
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4020
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD

4-114158729-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158729
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158729
    reference: chr 4
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.607-26C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.670-26C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.607-26C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.607-26C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.715-26C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.670-26C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.670-26C>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4011
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4031
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1992
  bin: 7.25e1
  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: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

4-114158741-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158741
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158741
    reference: chr 4
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.607-14C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.670-14C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.607-14C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.670-14C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.607-14C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.715-14C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.670-14C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4728
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-114158745-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158745
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158745
    reference: chr 4
allele count: 17
allele frequency: 1.400329489291598e-4
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.607-10A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.670-10A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.670-10A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.607-10A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.607-10A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.670-10A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.715-10A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6036
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4737
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3795
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34554
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-114158768-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158768
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158768
    reference: chr 4
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.683G>T
  hgvsp: ENSP00000264366.6:p.Arg228Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.620G>T
  hgvsp: ENSP00000421011.1:p.Arg207Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.620G>T
  hgvsp: ENSP00000423799.1:p.Arg207Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.683G>T
  hgvsp: ENSP00000378044.3:p.Arg228Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.683G>T
  hgvsp: ENSP00000349588.4:p.Arg228Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.620G>T
  hgvsp: ENSP00000421067.1:p.Arg207Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.728G>T
  hgvsp: ENSP00000424722.1:p.Arg243Met
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4728
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6041
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6117
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4030
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3796
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg228Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS

4-114158784-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158784
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158784
    reference: chr 4
allele count: 5
allele frequency: 4.118751853438334e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.630+6G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.693+6G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.693+6G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.630+6G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.738+6G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.630+6G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.693+6G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6040
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34545
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4030
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2172
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6103
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4020
  bin: 9.25e1
  variant carriers: 0
hgvs: c.693+6G>A
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/4-114158798-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158798
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158798
    reference: chr 4
allele count: 3
allele frequency: 2.471454698235381e-5
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.693+20C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.693+20C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.630+20C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.738+20C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.630+20C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.693+20C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.630+20C>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6040
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4028
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3787
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2172
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

4-114158807-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158807
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158807
    reference: chr 4
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.630+29A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.693+29A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.630+29A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.693+29A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.693+29A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.630+29A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.738+29A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6041
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2171
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5990
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4020
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1976
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

4-114158809-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158809
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158809
    reference: chr 4
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.693+31C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.693+31C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.630+31C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.630+31C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.738+31C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.693+31C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.630+31C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6041
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3943
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4022
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

4-114158814-CTTTAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114158814
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114158809
    reference: chr 4
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.693+40_693+44delATTTT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.738+40_738+44delATTTT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.630+40_630+44delATTTT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.693+40_693+44delATTTT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000423799
  ensembl transcript: ENST00000503271
  gene symbol: ANK2
  hgvsc: ENST00000503271.1:c.630+40_630+44delATTTT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.693+40_693+44delATTTT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.630+40_630+44delATTTT
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
reference allele: CTTTAT

GenotypeQuality
all individuals: 1508
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8961
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 671
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4340
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13890
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5051
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3913
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5651
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2793
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.92379082634303e-5
allele num: 11206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16172
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.737e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.51e-1

DP
type: SiteQuality
SIO_000300: 1.733691e6

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -6.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.79e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.798157946306095e-5
allele num: 10206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66308
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.289e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.52e-1

QD
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507113576079093e-5
allele num: 66352
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.492e0

DP
type: SiteQuality
SIO_000300: 2.15116e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -5.09e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.55e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.345e1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.792401096748923e-5
allele num: 10212
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66378
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.43e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

DP
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SIO_000300: 2.158635e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.53e-1

InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.66e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.16e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-2

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50652324565368e-5
allele num: 66378
num of homozygotes: 0

VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
SIO_000300: -7.3e-2

ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16767865483419e-4
allele num: 8564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
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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
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European (Finnish)
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num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 66406
num of homozygotes: 0

QD
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
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num of homozygotes: 0

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

Latino
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South Asian
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African
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allele frequency: 9.759906304899473e-4
allele num: 10246
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Other
type: Population
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num of homozygotes: 0

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

East Asian
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European (Non-Finnish)
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South Asian
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Latino
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allele num: 11560
num of homozygotes: 0

Other
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European (Finnish)
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InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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East Asian
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African
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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FS
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele num: 66728
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Other
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East Asian
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MQRankSum
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FS
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QD
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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African
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Latino
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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Other
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MQ
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InbreedingCoeff
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DP
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QD
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11576
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Other
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East Asian
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allele frequency: 0.0e0
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African
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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VQSLOD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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South Asian
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African
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European (Non-Finnish)
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East Asian
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allele num: 8650
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Latino
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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QD
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MQ
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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Latino
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South Asian
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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DP
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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ClippingRankSum
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MQRankSum
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QD
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MQ
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DP
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BaseQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Latino
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QD
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BaseQRankSum
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FS
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Latino
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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allele frequency: 1.512401693889897e-4
allele num: 6612
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Other
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VQSLOD
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MQ
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FS
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InbreedingCoeff
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DP
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MQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.64902266043937e-5
allele num: 11562
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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MQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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allele frequency: 0.0e0
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Latino
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Other
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allele frequency: 0.0e0
allele num: 908
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South Asian
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allele frequency: 6.06134076857801e-5
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European (Non-Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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FS
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ReadPosRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.012138919846983e-5
allele num: 66398
num of homozygotes: 0

South Asian
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DP
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BaseQRankSum
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

South Asian
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allele frequency: 6.079766536964981e-5
allele num: 16448
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African
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65944
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European (Finnish)
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Other
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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MQ
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QD
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BaseQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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allele frequency: 7.630791770954154e-5
allele num: 65524
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African
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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DP
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FS
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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Other
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 4.594884362076888e-5
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ClippingRankSum
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FS
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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South Asian
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East Asian
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InbreedingCoeff
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FS
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VQSLOD
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DP
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MQ
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QD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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DP
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BaseQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2891
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66068
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.610966057441253e-4
allele num: 11490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.302903e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e0

VQSLOD
type: SiteQuality
SIO_000300: 8.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-1

FS
type: SiteQuality
SIO_000300: 2.346e0

QD
type: SiteQuality
SIO_000300: 1.369e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
all individuals: 3659
bin: 9.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 7.110653877575721e-4
allele num: 66098
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.083465141744738e-5
allele num: 16438
num of homozygotes: 0

Latino
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allele count: 8
allele frequency: 6.960153123368715e-4
allele num: 11494
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.962143853357243e-5
allele num: 10038
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.98e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

QD
type: SiteQuality
SIO_000300: 1.592e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

DP
type: SiteQuality
SIO_000300: 2.306751e6

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.166861143523921e-4
allele num: 8570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66098
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.306751e6

QD
type: SiteQuality
SIO_000300: 1.592e1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.021787084881999e-5
allele num: 66186
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 1.373e1

FS
type: SiteQuality
SIO_000300: 2.031e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.84e-1

DP
type: SiteQuality
SIO_000300: 2.311494e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.81e0

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.977456990310461e-4
allele num: 10114
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.314e0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.354e1

FS
type: SiteQuality
SIO_000300: 1.148e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.05e-1

DP
type: SiteQuality
SIO_000300: 2.312376e6

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-1

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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.844457570387872e-5
allele num: 10158
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.731e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 2.314135e6

VQSLOD
type: SiteQuality
SIO_000300: 5.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e-1

QD
type: SiteQuality
SIO_000300: 1.417e1

MQ
type: SiteQuality
SIO_000300: 5.939e1

GenotypeQuality
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bin: 2.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503442884204829e-5
allele num: 66514
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 9.885e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -9.342e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.102e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502358703163967e-5
allele num: 66562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
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DP
type: SiteQuality
SIO_000300: 2.319568e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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ReadPosRankSum
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.28e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.56e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.495e0

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
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 24970
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variant carriers: 11

GenotypeQuality
all individuals: 2933
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.635922918434129e-4
allele num: 16502
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
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allele frequency: 3.002912825440678e-5
allele num: 66602
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African
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ClippingRankSum
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MQRankSum
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MQ
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DP
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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allele num: 66624
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Other
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InbreedingCoeff
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QD
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VQSLOD
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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MQ
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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Other
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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MQRankSum
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FS
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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East Asian
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.500060002400096e-5
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
type: SiteQuality
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ClippingRankSum
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DP
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InbreedingCoeff
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FS
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MQ
type: SiteQuality
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VQSLOD
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QD
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Latino
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allele frequency: 6.914433880726015e-4
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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Other
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BaseQRankSum
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FS
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DP
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QD
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ClippingRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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allele frequency: 3.023888720895071e-4
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Latino
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Other
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FS
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 66674
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Latino
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African
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East Asian
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European (Finnish)
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South Asian
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Other
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BaseQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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MQ
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DP
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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African
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Latino
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South Asian
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MQRankSum
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FS
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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QD
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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South Asian
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MQRankSum
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QD
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DP
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ClippingRankSum
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.054e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 5.869e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.321086e6

QD
type: SiteQuality
SIO_000300: 1.296e1

MQ
type: SiteQuality
SIO_000300: 5.932e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e0

VQSLOD
type: SiteQuality
SIO_000300: 3.88e-1

GenotypeQuality
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bin: 2.5e0
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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bin: 7.25e1
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GenotypeQuality
all individuals: 2404
bin: 8.75e1
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GenotypeQuality
all individuals: 24968
bin: 9.75e1
variant carriers: 2

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.84e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.328e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.268e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.401e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

FS
type: SiteQuality
SIO_000300: 1.762e0

DP
type: SiteQuality
SIO_000300: 2.320868e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.320392e6

VQSLOD
type: SiteQuality
SIO_000300: -1.654e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.474e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e0

FS
type: SiteQuality
SIO_000300: 1.087e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 1.401e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

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

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

African
type: Population
allele count: 15
allele frequency: 1.448435689455388e-3
allele num: 10356
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.88e0

VQSLOD
type: SiteQuality
SIO_000300: 2.81e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.515e1

DP
type: SiteQuality
SIO_000300: 2.319829e6

MQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-2

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.282e1

MQRankSum
type: SiteQuality
SIO_000300: -9.25e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.373e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

FS
type: SiteQuality
SIO_000300: 9.755000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

DP
type: SiteQuality
SIO_000300: 2.318069e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.373e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

DP
type: SiteQuality
SIO_000300: 2.318069e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

FS
type: SiteQuality
SIO_000300: 9.755000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

MQRankSum
type: SiteQuality
SIO_000300: -9.25e-1

GenotypeQuality
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bin: 2.25e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003093185981561e-5
allele num: 66598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

FS
type: SiteQuality
SIO_000300: 8.071e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
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DP
type: SiteQuality
SIO_000300: 2.317043e6

MQRankSum
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
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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: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66592
num of homozygotes: 0

African
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66588
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

Latino
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allele frequency: 1.730702665282105e-4
allele num: 11556
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503895088278642e-5
allele num: 66494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.303883e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.989e0

MQ
type: SiteQuality
SIO_000300: 5.814e1

QD
type: SiteQuality
SIO_000300: 1.201e1

MQRankSum
type: SiteQuality
SIO_000300: 2.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.34e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2824
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GenotypeQuality
all individuals: 2394
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507159005275056e-5
allele num: 66350
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.13e-1

DP
type: SiteQuality
SIO_000300: 2.306315e6

MQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

FS
type: SiteQuality
SIO_000300: 3.191e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.404e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 18
bin: 4.25e1
variant carriers: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.198861081972126e-4
allele num: 66730
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.463e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

DP
type: SiteQuality
SIO_000300: 3.37021e6

VQSLOD
type: SiteQuality
SIO_000300: 6.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.523e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.89e0

GenotypeQuality
all individuals: 1996
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.075e-1

QD
type: SiteQuality
SIO_000300: 1.447e1

MQ
type: SiteQuality
SIO_000300: 5.895e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

DP
type: SiteQuality
SIO_000300: 3.370088e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e0

GenotypeQuality
all individuals: 1990
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.214e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e0

MQ
type: SiteQuality
SIO_000300: 5.73e1

DP
type: SiteQuality
SIO_000300: 3.370172e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.18e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

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

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4021
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GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
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: 11574
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.3e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

QD
type: SiteQuality
SIO_000300: 1.38e1

DP
type: SiteQuality
SIO_000300: 3.370097e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.1e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.888e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.124e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
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allele num: 11576
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.84e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6100
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

East Asian
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allele num: 8648
num of homozygotes: 0

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

GenotypeQuality
all individuals: 4020
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4030
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4010
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34553
bin: 9.75e1
variant carriers: 1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.18e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.387e-1

FS
type: SiteQuality
SIO_000300: 9.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

QD
type: SiteQuality
SIO_000300: 8.49e0

DP
type: SiteQuality
SIO_000300: 3.370276e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.291e0

GenotypeQuality
all individuals: 1994
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2171
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4030
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4009
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4020
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6121
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

African
type: Population
allele count: 16
allele frequency: 1.537574476263694e-3
allele num: 10406
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.370998e6

QD
type: SiteQuality
SIO_000300: 1.157e1

MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

FS
type: SiteQuality
SIO_000300: 5.31e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: 2.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.01e-1

GenotypeQuality
all individuals: 1994
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2172
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34547
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4020
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4012
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996973057212216e-5
allele num: 66734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 3.370167e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 1.086e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.323e0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4010
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3796
bin: 7.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 5
allele frequency: 3.028467595396729e-4
allele num: 16510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.432e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.122e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.47e-1

DP
type: SiteQuality
SIO_000300: 3.370049e6

QD
type: SiteQuality
SIO_000300: 1.154e1

GenotypeQuality
all individuals: 4020
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3992
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6049
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1986
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34543
bin: 9.75e1
variant carriers: 3

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495863805299125e-5
allele num: 66728
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.913e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.369133e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -2.536e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

FS
type: SiteQuality
SIO_000300: 5.157e0

QD
type: SiteQuality
SIO_000300: 1.172e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.528e0

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

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

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4024
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34540
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3956
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3782
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.26e0

VQSLOD
type: SiteQuality
SIO_000300: 1.57e-1

QD
type: SiteQuality
SIO_000300: 1.724e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: 2.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

DP
type: SiteQuality
SIO_000300: 3.367624e6

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34537
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5935
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4019
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.898e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

DP
type: SiteQuality
SIO_000300: 3.366787e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

FS
type: SiteQuality
SIO_000300: 2.86e0

QD
type: SiteQuality
SIO_000300: 8.32e0

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1