6-32323464-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32323464
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32323464
    reference: chr 6
allele count: 17
allele frequency: 1.440971044958297e-4
allele num: 117976
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.218-18T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.230-18T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.218-18T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.201-5T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.197-18T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.218-18T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.218-18T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.197-18T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13824
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6531
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20899
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6119
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2983
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25920
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1369
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8346
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 7.5e0
  variant carriers: 0
hgvs: c.201-5T>C
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ

6-32323478-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32323478
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32323478
    reference: chr 6
allele count: 1
allele frequency: 8.523259976475802e-6
allele num: 117326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.197-32T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.197-32T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.230-32T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.201-19T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.218-32T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.218-32T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.218-32T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.218-32T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4226
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2410
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2912
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

6-32323479-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32323479
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32323479
    reference: chr 6
allele count: 1
allele frequency: 8.525149190110827e-6
allele num: 117300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.197-33A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.201-20A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.218-33A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.230-33A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.218-33A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.197-33A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.218-33A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.218-33A>G
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19743
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7923
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2907
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

6-32323483-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32323483
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32323482
    reference: chr 6
allele count: 1
allele frequency: 8.536647829130458e-6
allele num: 117142
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.218-38delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.197-38delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.218-38delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.201-25delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.218-38delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.218-38delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.197-38delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.230-38delT
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6044
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2123
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7770
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: GA
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

6-32323487-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32323487
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32323487
    reference: chr 6
allele count: 1
allele frequency: 8.548615979072987e-6
allele num: 116978
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.230-41A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.201-28A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.218-41A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.197-41A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.218-41A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.197-41A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.218-41A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.218-41A>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20998
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1879
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7619
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

6-32323497-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32323497
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32323497
    reference: chr 6
allele count: 90
allele frequency: 7.748334108166745e-4
allele num: 116154
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.218-51C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.218-51C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.218-51C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.197-51C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.201-38C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.197-51C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.218-51C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.230-51C>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8302
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 13708
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10301
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5807
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3572
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-32323504-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32323504
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32323504
    reference: chr 6
allele count: 3
allele frequency: 2.590852563216803e-5
allele num: 115792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.230-58A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.218-58A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.218-58A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.218-58A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.201-45A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.197-58A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.197-58A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.218-58A>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11662
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9135
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11221
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3901
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3038
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2484
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

6-32323508-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32323508
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32323508
    reference: chr 6
allele count: 2
allele frequency: 1.732801940738174e-5
allele num: 115420
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.218-62T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.218-62T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.230-62T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.197-62T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.201-49T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.197-62T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.218-62T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.218-62T>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8157
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8508
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2344
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1346
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4802
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3943
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3121
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-32333084-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333084
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333084
    reference: chr 6
allele count: 4
allele frequency: 2.656395271616417e-4
allele num: 15058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+860G>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+966G>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+966G>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+966G>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+962G>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+860G>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+860G>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+860G>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1557
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

6-32333093-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333093
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333093
    reference: chr 6
allele count: 8834
allele frequency: 5.670817820002567e-1
allele num: 15578
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+851T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+851T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+851T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+851T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+957T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+957T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+953T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+957T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 3.75e1
  variant carriers: 603
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 275
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 667
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 779
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.25e1
  variant carriers: 801
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 2.75e1
  variant carriers: 195
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 2.5e0
  variant carriers: 299
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.5e0
  variant carriers: 392
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 494
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 4.75e1
  variant carriers: 924
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.25e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 193
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 3.25e1
  variant carriers: 415
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 326
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 96
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 2.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 6.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.25e1
  variant carriers: 85
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 35
num of homozygotes: 2530
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-32333098-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333098
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333098
    reference: chr 6
allele count: 8897
allele frequency: 5.680628272251309e-1
allele num: 15662
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+846G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+952G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+846G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+952G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+846G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+948G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+846G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+952G>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 2.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.75e1
  variant carriers: 220
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 152
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 6.25e1
  variant carriers: 686
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 2.5e0
  variant carriers: 276
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 5.25e1
  variant carriers: 818
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 289
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.75e1
  variant carriers: 720
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.5e0
  variant carriers: 369
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 3.75e1
  variant carriers: 427
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.75e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.25e1
  variant carriers: 574
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 342
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 146
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.75e1
  variant carriers: 494
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.25e1
  variant carriers: 249
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 5.75e1
  variant carriers: 743
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 9.25e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.75e1
  variant carriers: 89
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 8.25e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 8.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 7.5e0
  variant carriers: 150
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 6.25e1
  variant carriers: 30
num of homozygotes: 2549
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

6-32333104-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333104
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333104
    reference: chr 6
allele count: 2
allele frequency: 1.281886937572106e-4
allele num: 15602
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+946C>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+946C>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+946C>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+840C>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+942C>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+840C>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+840C>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+840C>G
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5386
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

6-32333106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333106
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333106
    reference: chr 6
allele count: 1
allele frequency: 6.40450877417702e-5
allele num: 15614
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+944G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+940G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+838G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+944G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+838G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+838G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+944G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+838G>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1738
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

6-32333195-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333195
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333195
    reference: chr 6
allele count: 8966
allele frequency: 5.664644933030073e-1
allele num: 15828
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+749T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+855T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+749T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+855T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+851T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+749T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+855T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+749T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.75e1
  variant carriers: 775
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 258
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.25e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 396
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 358
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.25e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 2.75e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 7.5e0
  variant carriers: 399
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.25e1
  variant carriers: 665
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 157
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 2.5e0
  variant carriers: 329
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 692
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.25e1
  variant carriers: 564
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.25e1
  variant carriers: 309
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 130
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 477
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 215
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.25e1
  variant carriers: 763
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 111
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.25e1
  variant carriers: 92
genotype quality: GenotypeQuality
  all individuals: 6652
  bin: 9.75e1
  variant carriers: 6031
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 1.75e1
  variant carriers: 93
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.25e1
  variant carriers: 56
num of homozygotes: 2591
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

6-32333270-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333270
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333270
    reference: chr 6
allele count: 1
allele frequency: 6.974473427256242e-5
allele num: 14338
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+674A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+674A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+776A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+780A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+780A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+674A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+780A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+674A>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2571
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

6-32333273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333273
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333273
    reference: chr 6
allele count: 1
allele frequency: 6.985191394244202e-5
allele num: 14316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+777C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+671C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+777C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+773C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+671C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+671C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+671C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+777C>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum

6-32333299-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333299
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333299
    reference: chr 6
allele count: 1768
allele frequency: 1.240179573512907e-1
allele num: 14256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+645G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+645G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+751G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+645G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+751G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+747G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+645G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+751G>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 8.75e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 9.75e1
  variant carriers: 813
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 2.5e0
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.25e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 6.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 7.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.25e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 5.25e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 8.25e1
  variant carriers: 2
num of homozygotes: 115
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

6-32333308-TCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333308
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333305
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 14248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+739_229+741delGAG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+633_217+635delGAG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+633_217+635delGAG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+735_200+737delGAG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+633_217+635delGAG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+633_217+635delGAG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+739_196+741delGAG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+739_196+741delGAG
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2789
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: TCTC
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP

6-32333311-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333311
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333311
    reference: chr 6
allele count: 1
allele frequency: 7.019514249613927e-5
allele num: 14246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+633G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+739G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+633G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+735G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+633G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+739G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+739G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+633G>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3061
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6755
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

6-32333314-A-ATGCTGGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333314
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333321
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 14248
alternate allele: ATGCTGGG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6756
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum

6-32333316-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333316
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333316
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 14248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+628G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+628G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+628G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+734G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+730G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+628G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+734G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+734G>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6756
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

6-32333322-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333322
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333323
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 14248
alternate allele: AG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+621_217+622insC
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+621_217+622insC
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+723_200+724insC
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+727_229+728insC
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+621_217+622insC
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+621_217+622insC
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+727_196+728insC
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+727_196+728insC
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

6-32333323-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333323
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333323
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 14248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+723T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+727T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+727T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+621T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+621T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+621T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+621T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+727T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

6-32333341-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333341
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333341
    reference: chr 6
allele count: 1362
allele frequency: 9.553872053872053e-2
allele num: 14256
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+603T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+603T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+603T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+705T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+709T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+709T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+709T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+603T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 2.5e0
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 6.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 9.75e1
  variant carriers: 571
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 8.25e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.25e1
  variant carriers: 77
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 6.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1977
  bin: 7.5e0
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.25e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 6.25e1
  variant carriers: 8
num of homozygotes: 100
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

6-32333350-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333350
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333350
    reference: chr 6
allele count: 1
allele frequency: 7.017543859649122e-5
allele num: 14250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+700C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+696C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+700C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+700C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+594C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+594C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+594C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+594C>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

6-32333740-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333740
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333740
    reference: chr 6
allele count: 1
allele frequency: 5.48065329387263e-5
allele num: 18246
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+310A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+310A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+306A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+204A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+310A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+204A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+204A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+204A>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17553
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2955
  bin: 2.5e0
  variant carriers: 0
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: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

6-32333777-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333777
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333777
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 18952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+167G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+167G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+273G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+269G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+273G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+167G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+167G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+273G>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26824
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24663
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2144
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1576
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

6-32333781-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333781
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333781
    reference: chr 6
allele count: 67
allele frequency: 3.508588186007541e-3
allele num: 19096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+163A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+163A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+269A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+269A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+269A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+163A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+265A>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+163A>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28142
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 9.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26085
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2032
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4262
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 2
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

6-32333784-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333784
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333784
    reference: chr 6
allele count: 208
allele frequency: 1.086048454469507e-2
allele num: 19152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+160G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+266G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+160G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+160G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+160G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+262G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+266G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+266G>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28957
  bin: 2.5e0
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 7.5e0
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 9.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 26785
  bin: 7.5e0
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 4264
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 6.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1449
  bin: 9.75e1
  variant carriers: 218
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 8.75e1
  variant carriers: 8
num of homozygotes: 3
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

6-32333785-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333785
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333785
    reference: chr 6
allele count: 1
allele frequency: 5.200208008320333e-5
allele num: 19230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+265C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+159C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+159C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+261C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+265C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+265C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+159C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+159C>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29702
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3427
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28104
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4376
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-32333827-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333827
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333827
    reference: chr 6
allele count: 1718
allele frequency: 7.965504451038576e-2
allele num: 21568
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+223T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+219T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+223T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+117T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+117T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+117T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+117T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+223T>G
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 16219
  bin: 2.5e0
  variant carriers: 500
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 2.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 10567
  bin: 7.5e0
  variant carriers: 1994
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 5.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 3.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.75e1
  variant carriers: 210
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 1.25e1
  variant carriers: 773
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 9.75e1
  variant carriers: 210
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 1.25e1
  variant carriers: 118
genotype quality: GenotypeQuality
  all individuals: 2652
  bin: 6.25e1
  variant carriers: 156
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.25e1
  variant carriers: 143
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 7.25e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 9.25e1
  variant carriers: 186
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 6069
  bin: 2.5e0
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 3.25e1
  variant carriers: 57
num of homozygotes: 68
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

6-32333837-T-TTTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333837
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333840
    reference: chr 6
allele count: 36221
allele frequency: 8.278707259096727e-1
allele num: 43752
alternate allele: TTTC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+210_196+212dupGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+104_217+106dupGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+210_229+212dupGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+104_217+106dupGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+104_217+106dupGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+210_196+212dupGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+104_217+106dupGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+206_200+208dupGAA
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 642
genotype depth: GenotypeDepth
  all individuals: 22873
  bin: 7.5e0
  variant carriers: 19655
genotype depth: GenotypeDepth
  all individuals: 8435
  bin: 2.5e0
  variant carriers: 6160
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 6.25e1
  variant carriers: 413
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 298
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 2.25e1
  variant carriers: 977
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 9.75e1
  variant carriers: 928
genotype depth: GenotypeDepth
  all individuals: 9806
  bin: 1.25e1
  variant carriers: 9458
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 1.75e1
  variant carriers: 2616
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 1031
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 146
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 3.25e1
  variant carriers: 845
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 4.25e1
  variant carriers: 1034
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 215
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 2.75e1
  variant carriers: 735
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 971
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.25e1
  variant carriers: 887
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 8.75e1
  variant carriers: 473
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 7.75e1
  variant carriers: 476
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 6.75e1
  variant carriers: 307
genotype quality: GenotypeQuality
  all individuals: 3625
  bin: 2.5e0
  variant carriers: 56
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.25e1
  variant carriers: 332
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 3.75e1
  variant carriers: 2669
genotype quality: GenotypeQuality
  all individuals: 4228
  bin: 1.75e1
  variant carriers: 4125
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 9.25e1
  variant carriers: 283
num of homozygotes: 14834
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

6-32333837-TTTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333837
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333834
    reference: chr 6
allele count: 1
allele frequency: 2.285609800694825e-5
allele num: 43752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+104_217+106delGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+210_196+212delGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+104_217+106delGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+210_229+212delGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+206_200+208delGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+210_196+212delGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+104_217+106delGAA
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+104_217+106delGAA
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22873
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9806
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2328
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6772
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5455
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: TTTC
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP

6-32333894-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333894
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333894
    reference: chr 6
allele count: 773
allele frequency: 8.01833948798805e-3
allele num: 96404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+156T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+50T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+50T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+152T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+50T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+156T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+50T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+156T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 3.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 3.25e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 11376
  bin: 1.75e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9188
  bin: 1.25e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9661
  bin: 2.75e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 11292
  bin: 2.25e1
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 7.5e0
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3474
  bin: 5.25e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 3972
  bin: 3.25e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 7.5e0
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 1.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 3997
  bin: 9.75e1
  variant carriers: 430
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 7.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 7.25e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 1256
  bin: 8.25e1
  variant carriers: 18
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

6-32333895-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333895
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333895
    reference: chr 6
allele count: 2
allele frequency: 1.930762844399822e-5
allele num: 103586
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+49T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+155T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+155T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+151T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+49T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+49T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+49T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+155T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12033
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3703
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4184
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1202
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3398
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2399
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5122
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/6-32333897-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333897
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333897
    reference: chr 6
allele count: 1
allele frequency: 9.646922631680493e-6
allele num: 103660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+149T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+47T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+153T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+153T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+153T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+47T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+47T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+47T>G
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10436
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5240
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2083
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1726
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2861
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2259
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS

6-32333903-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333903
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333903
    reference: chr 6
allele count: 1
allele frequency: 9.617049104652728e-6
allele num: 103982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+41C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+147C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+41C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+41C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+143C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+147C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+41C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+147C>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8669
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1152
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5821
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3063
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3705
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

6-32333909-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333909
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333909
    reference: chr 6
allele count: 51
allele frequency: 5.189149589955434e-4
allele num: 98282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+141G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+35G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+137G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+35G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+141G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+35G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+141G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+35G>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 12622
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15687
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7548
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3409
  bin: 3.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 4377
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2940
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1884
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1906
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 1.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 16583
  bin: 6.25e1
  variant carriers: 2
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum

6-32333914-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333914
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333914
    reference: chr 6
allele count: 1
allele frequency: 9.485866059571238e-6
allele num: 105420
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+132T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+30T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+30T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+136T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+30T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+30T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+136T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+136T>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5804
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4268
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2076
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1093
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2512
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21058
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5233
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

6-32333920-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333920
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333920
    reference: chr 6
allele count: 1
allele frequency: 9.446795646916565e-6
allele num: 105856
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+130T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+130T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+130T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+24T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+24T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+24T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+24T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+126T>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14116
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18808
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2501
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4289
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

6-32333935-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333935
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333935
    reference: chr 6
allele count: 1
allele frequency: 9.185773074661964e-6
allele num: 108864
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+9A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+9A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+115A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+111A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+9A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+9A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+115A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+115A>G
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2733
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3816
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2028
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2927
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

6-32333936-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333936
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333936
    reference: chr 6
allele count: 428
allele frequency: 3.922790680622514e-3
allele num: 109106
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+114T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.217+8T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.217+8T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.217+8T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.217+8T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+114T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+114T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+110T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 6147
  bin: 3.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 1.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 3.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 1.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 22903
  bin: 2.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 14913
  bin: 2.75e1
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 3693
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2714
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
hgvs: c.217+8T>C
num of homozygotes: 2
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/6-32333946-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333946
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333946
    reference: chr 6
allele count: 2
allele frequency: 1.811069255288322e-5
allele num: 110432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.215G>T
  hgvsp: ENSP00000432566.1:p.Arg72Leu
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+104G>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.215G>T
  hgvsp: ENSP00000364155.4:p.Arg72Leu
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.215G>T
  hgvsp: ENSP00000415517.2:p.Arg72Leu
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+100G>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+104G>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+104G>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.215G>T
  hgvsp: ENSP00000431199.1:p.Arg72Leu
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15527
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30374
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg72Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-32333946-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333946
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333946
    reference: chr 6
allele count: 3
allele frequency: 2.716603882932483e-5
allele num: 110432
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+100G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+104G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.215G>A
  hgvsp: ENSP00000431199.1:p.Arg72Gln
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.215G>A
  hgvsp: ENSP00000364155.4:p.Arg72Gln
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.215G>A
  hgvsp: ENSP00000432566.1:p.Arg72Gln
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+104G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+104G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.215G>A
  hgvsp: ENSP00000415517.2:p.Arg72Gln
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24108
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6821
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30374
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg72Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

6-32333947-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333947
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333947
    reference: chr 6
allele count: 3
allele frequency: 2.712624554677469e-5
allele num: 110594
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+99C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+103C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.214C>T
  hgvsp: ENSP00000415517.2:p.Arg72Ter
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.214C>T
  hgvsp: ENSP00000432566.1:p.Arg72Ter
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.214C>T
  hgvsp: ENSP00000431199.1:p.Arg72Ter
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.214C>T
  hgvsp: ENSP00000364155.4:p.Arg72Ter
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+103C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+103C>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15616
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6412
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30552
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg72Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP

6-32333947-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333947
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333947
    reference: chr 6
allele count: 2
allele frequency: 1.808416369784979e-5
allele num: 110594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.214C>A
  hgvsp: ENST00000375015.4:c.214C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+99C>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.214C>A
  hgvsp: ENST00000534588.1:c.214C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+103C>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.214C>A
  hgvsp: ENST00000447241.2:c.214C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+103C>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+103C>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.214C>A
  hgvsp: ENST00000533191.1:c.214C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24201
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15616
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2823
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2808
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg72Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

6-32333955-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333955
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333955
    reference: chr 6
allele count: 47676
allele frequency: 4.203787958946143e-1
allele num: 113412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.206A>G
  hgvsp: ENSP00000364155.4:p.Tyr69Cys
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.206A>G
  hgvsp: ENSP00000432566.1:p.Tyr69Cys
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+95A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+95A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+95A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.206A>G
  hgvsp: ENSP00000415517.2:p.Tyr69Cys
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.206A>G
  hgvsp: ENSP00000431199.1:p.Tyr69Cys
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+91A>G
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 702
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 4.75e1
  variant carriers: 3869
genotype depth: GenotypeDepth
  all individuals: 5000
  bin: 3.75e1
  variant carriers: 4722
genotype depth: GenotypeDepth
  all individuals: 12137
  bin: 2.25e1
  variant carriers: 2720
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 7.5e0
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 6.75e1
  variant carriers: 1128
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.75e1
  variant carriers: 508
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 1.75e1
  variant carriers: 1520
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 369
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 9.75e1
  variant carriers: 1380
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 2.5e0
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 1.25e1
  variant carriers: 582
genotype depth: GenotypeDepth
  all individuals: 6207
  bin: 3.25e1
  variant carriers: 4495
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 2.75e1
  variant carriers: 3673
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 5.25e1
  variant carriers: 2938
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 4.25e1
  variant carriers: 4393
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.75e1
  variant carriers: 2097
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 291
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 228
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 6.25e1
  variant carriers: 1511
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 7.5e0
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 15994
  bin: 6.25e1
  variant carriers: 331
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 7.75e1
  variant carriers: 473
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 5.75e1
  variant carriers: 190
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.5e0
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 27
hgvs: p.Tyr69Cys
num of homozygotes: 10614
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

6-32333970-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333970
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333970
    reference: chr 6
allele count: 1
allele frequency: 8.791981712678038e-6
allele num: 113740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+80C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.197-6C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+80C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.197-6C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.197-6C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.197-6C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+76C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+80C>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 2.25e1
  variant carriers: 0
hgvs: c.197-6C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-32333983-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333983
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333983
    reference: chr 6
allele count: 1
allele frequency: 8.77531678893608e-6
allele num: 113956
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+67T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+67T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.197-19T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.197-19T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.197-19T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+63T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+67T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.197-19T>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1277
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

6-32333984-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333984
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333984
    reference: chr 6
allele count: 1
allele frequency: 8.774546794658055e-6
allele num: 113966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+66A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+66A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+66A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.197-20A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.197-20A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+62A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.197-20A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.197-20A>G
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43402
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD

6-32333993-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32333993
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32333993
    reference: chr 6
allele count: 1
allele frequency: 8.761324011284586e-6
allele num: 114138
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.197-29A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+57A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.197-29A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+57A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.197-29A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+53A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+57A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.197-29A>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6223
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43425
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-32334000-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334000
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334000
    reference: chr 6
allele count: 1
allele frequency: 8.748906386701662e-6
allele num: 114300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+46A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+50A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.197-36A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+50A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.197-36A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.197-36A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+50A>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.197-36A>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

6-32334034-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334034
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334034
    reference: chr 6
allele count: 2
allele frequency: 1.739493459504592e-5
allele num: 114976
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.196+16G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.196+16G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.196+16G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+16G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+16G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+16G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.196+16G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+12G>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1233
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/6-32334035-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334035
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334035
    reference: chr 6
allele count: 2
allele frequency: 1.739160681055323e-5
allele num: 114998
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.196+15T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.196+15T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.196+15T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.196+15T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.229+15T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.196+15T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.196+15T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.200+11T>G
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6245
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP

6-32334073-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334073
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334073
    reference: chr 6
allele count: 5
allele frequency: 4.354111151749482e-5
allele num: 114834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.173G>A
  hgvsp: ENSP00000364146.4:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.173G>A
  hgvsp: ENSP00000435103.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.173G>A
  hgvsp: ENSP00000431199.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.206G>A
  hgvsp: ENSP00000432814.1:p.Arg69Gln
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.173G>A
  hgvsp: ENSP00000415517.2:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.173G>A
  hgvsp: ENSP00000411164.2:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.173G>A
  hgvsp: ENSP00000364155.4:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.173G>A
  hgvsp: ENSP00000432566.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg58Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

6-32334074-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334074
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334074
    reference: chr 6
allele count: 1
allele frequency: 8.710194411539265e-6
allele num: 114808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.172C>T
  hgvsp: ENSP00000431199.1:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.205C>T
  hgvsp: ENSP00000432814.1:p.Arg69Ter
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.172C>T
  hgvsp: ENSP00000364146.4:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.172C>T
  hgvsp: ENSP00000435103.1:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.172C>T
  hgvsp: ENSP00000415517.2:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.172C>T
  hgvsp: ENSP00000364155.4:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.172C>T
  hgvsp: ENSP00000411164.2:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.172C>T
  hgvsp: ENSP00000432566.1:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg58Ter
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

6-32334090-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334090
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334090
    reference: chr 6
allele count: 1
allele frequency: 8.741105924721597e-6
allele num: 114402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.200-11T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-11T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-11T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-11T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-11T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-11T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-11T>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-11T>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6191
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

6-32334091-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334091
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334091
    reference: chr 6
allele count: 2
allele frequency: 1.748282312627843e-5
allele num: 114398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-12C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-12C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-12C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-12C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-12C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.200-12C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-12C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-12C>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46296
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

6-32334114-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334114
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334114
    reference: chr 6
allele count: 1
allele frequency: 8.887150957146158e-6
allele num: 112522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-35G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-35G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-35G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.200-35G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-35G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-35G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-35G>A
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-35G>A
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6013
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44353
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

6-32334127-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334127
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334127
    reference: chr 6
allele count: 1
allele frequency: 9.200139842125601e-6
allele num: 108694
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-48C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-48C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-48C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.199+37C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-48C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-48C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-48C>T
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-48C>T
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5087
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5676
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ

6-32334131-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334131
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334131
    reference: chr 6
allele count: 2
allele frequency: 1.868390568364411e-5
allele num: 107044
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-52T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-52T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-52T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.199+33T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-52T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-52T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-52T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-52T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16619
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39626
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5553
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

6-32334148-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334148
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334148
    reference: chr 6
allele count: 1
allele frequency: 1.04753723994888e-5
allele num: 95462
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.199+16T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-69T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-69T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-69T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-69T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-69T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-69T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-69T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8778
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29022
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-32334149-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334149
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334149
    reference: chr 6
allele count: 7
allele frequency: 7.449661572517134e-5
allele num: 93964
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-70A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-70A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-70A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.199+15A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-70A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-70A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-70A>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-70A>G
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17510
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12303
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

6-32334186-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334186
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334186
    reference: chr 6
allele count: 1
allele frequency: 1.570105197048202e-5
allele num: 63690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-107T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-107T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.177T>C
  hgvsp: ENST00000532023.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-107T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-107T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-107T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-107T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-107T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18847
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17083
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1586
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser59Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

6-32334205-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334205
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334205
    reference: chr 6
allele count: 1
allele frequency: 2.292421255329879e-5
allele num: 43622
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-126T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-126T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.167-9T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-126T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-126T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-126T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-126T>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-126T>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13516
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12687
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20029
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22091
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

6-32334208-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334208
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334208
    reference: chr 6
allele count: 1
allele frequency: 2.434867299732165e-5
allele num: 41070
alternate allele: A
canonical: false
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13881
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12028
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14906
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20909
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2131
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3301
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2346
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3810
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2540
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3248
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10582
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 18352
  num of homozygotes: 0
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

6-32334208-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334208
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334209
    reference: chr 6
allele count: 1
allele frequency: 2.434867299732165e-5
allele num: 41070
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-130dupT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.167-13dupT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-130dupT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-130dupT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-130dupT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-130dupT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-130dupT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-130dupT
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 12028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13881
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20909
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3810
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14906
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

6-32334208-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334208
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334207
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 41070
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.167-13delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-130delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-130delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-130delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-130delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-130delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-130delT
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-130delT
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13881
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20371
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2131
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3301
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2346
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20909
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: GA
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/6-32334215-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334215
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334215
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 37070
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-136T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-136T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.167-19T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-136T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-136T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-136T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-136T>G
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-136T>G
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14545
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21370
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16072
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16375
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2045
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3105
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4152
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/6-32334215-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334215
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334214
    reference: chr 6
allele count: 1
allele frequency: 2.697599136768276e-5
allele num: 37070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-137delG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-137delG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-137delG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.167-20delG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-137delG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-137delG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-137delG
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-137delG
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14545
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4152
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1009
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16072
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: AC
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

6-32334224-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32334224
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 32334224
    reference: chr 6
allele count: 14864
allele frequency: 4.63110667996012e-1
allele num: 32096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000411164
  ensembl transcript: ENST00000442822
  gene symbol: C6orf10
  hgvsc: ENST00000442822.2:c.167-145G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364155
  ensembl transcript: ENST00000375015
  gene symbol: C6orf10
  hgvsc: ENST00000375015.4:c.167-145G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000415517
  ensembl transcript: ENST00000447241
  gene symbol: C6orf10
  hgvsc: ENST00000447241.2:c.167-145G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432566
  ensembl transcript: ENST00000534588
  gene symbol: C6orf10
  hgvsc: ENST00000534588.1:c.167-145G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000432814
  ensembl transcript: ENST00000532023
  gene symbol: C6orf10
  hgvsc: ENST00000532023.1:c.167-28G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000431199
  ensembl transcript: ENST00000533191
  gene symbol: C6orf10
  hgvsc: ENST00000533191.1:c.167-145G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000364146
  ensembl transcript: ENST00000375007
  gene symbol: C6orf10
  hgvsc: ENST00000375007.4:c.167-145G>C
  variant of: http://identifiers.org/hgnc/13922
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204296
  ensembl protein: ENSP00000435103
  ensembl transcript: ENST00000527965
  gene symbol: C6orf10
  hgvsc: ENST00000527965.1:c.167-145G>C
  variant of: http://identifiers.org/hgnc/13922
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 2.25e1
  variant carriers: 850
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 179
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.75e1
  variant carriers: 325
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 915
genotype depth: GenotypeDepth
  all individuals: 21478
  bin: 7.5e0
  variant carriers: 11719
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14016
  bin: 2.5e0
  variant carriers: 3776
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 2.75e1
  variant carriers: 853
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 4.25e1
  variant carriers: 549
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 3.75e1
  variant carriers: 830
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8023
  bin: 1.25e1
  variant carriers: 5250
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 1.75e1
  variant carriers: 1629
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 6.75e1
  variant carriers: 692
genotype quality: GenotypeQuality
  all individuals: 9578
  bin: 7.5e0
  variant carriers: 1297
genotype quality: GenotypeQuality
  all individuals: 1854
  bin: 2.75e1
  variant carriers: 1378
genotype quality: GenotypeQuality
  all individuals: 11651
  bin: 9.75e1
  variant carriers: 11550
num of homozygotes: 3396
reference allele: C

GenotypeQuality
all individuals: 341
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8508
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 1815
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3143
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4284
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.053518752633797e-4
allele num: 9492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.462296091104955e-4
allele num: 64980
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 5.278e0

MQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.68e-1

DP
type: SiteQuality
SIO_000300: 1.983406e6

QD
type: SiteQuality
SIO_000300: 1.307e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeQuality
all individuals: 92
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23511
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8486
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1365
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2125
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7940
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3123
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.13195977434388e-5
allele num: 16308
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 3.514e0

DP
type: SiteQuality
SIO_000300: 1.948514e6

VQSLOD
type: SiteQuality
SIO_000300: 3.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.03e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.43e0

QD
type: SiteQuality
SIO_000300: 1.28e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.185e0

GenotypeQuality
all individuals: 2125
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4219
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3122
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2427
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23718
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1365
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8486
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 257
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.54813140539369e-5
allele num: 64594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.0e0

DP
type: SiteQuality
SIO_000300: 1.948123e6

QD
type: SiteQuality
SIO_000300: 6.1e0

GenotypeQuality
all individuals: 22641
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8485
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 301
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2877
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3107
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4184
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.844861135680169e-5
allele num: 11306
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16294
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.504e0

MQ
type: SiteQuality
SIO_000300: 6.107e1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.06e-1

DP
type: SiteQuality
SIO_000300: 1.931187e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

QD
type: SiteQuality
SIO_000300: 1.199e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.759e0

GenotypeQuality
all individuals: 8479
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 165
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4171
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2734
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2846
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3101
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2121
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11294
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551975665021572e-5
allele num: 64434
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.075e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.209e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

FS
type: SiteQuality
SIO_000300: 2.095e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.13e-1

DP
type: SiteQuality
SIO_000300: 1.909088e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

GenotypeQuality
all individuals: 2646
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3942
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1848
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2622
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8530
bin: 9.75e1
variant carriers: 89

GenotypeQuality
all individuals: 2988
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14194
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3046
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 7
allele frequency: 6.217800675075502e-4
allele num: 11258
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.20627261761158e-4
allele num: 8290
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.553498704183636e-4
allele num: 16206
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.202643171806167e-4
allele num: 9080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 71
allele frequency: 1.109548366932333e-3
allele num: 63990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

QD
type: SiteQuality
SIO_000300: 1.364e1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.821001e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.561e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.95e-1

GenotypeQuality
all individuals: 1525
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3905
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5434
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4282
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2584
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8459
bin: 9.75e1
variant carriers: 3

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.633720930232558e-4
allele num: 8256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9006
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16166
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.498e0

FS
type: SiteQuality
SIO_000300: 1.26e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.312e1

DP
type: SiteQuality
SIO_000300: 1.79404e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.42e-1

GenotypeQuality
all individuals: 815
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5133
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1530
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4760
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7109
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3893
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2419
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3041
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8456
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8956
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11228
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.144258583825934e-5
allele num: 63608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8214
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

QD
type: SiteQuality
SIO_000300: 1.169e1

MQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

DP
type: SiteQuality
SIO_000300: 1.783916e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 392
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1640
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 5.649717514124294e-3
allele num: 708
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -7.34e-1

FS
type: SiteQuality
SIO_000300: 8.6e-1

QD
type: SiteQuality
SIO_000300: 1.631e1

DP
type: SiteQuality
SIO_000300: 2.66094e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.53e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

MQ
type: SiteQuality
SIO_000300: 5.819e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.84e-1

GenotypeQuality
all individuals: 62
bin: 3.75e1
variant carriers: 49

GenotypeQuality
all individuals: 149
bin: 8.25e1
variant carriers: 31

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 25

GenotypeQuality
all individuals: 745
bin: 7.5e0
variant carriers: 152

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 88

GenotypeQuality
all individuals: 214
bin: 6.25e1
variant carriers: 30

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 49

GenotypeQuality
all individuals: 6815
bin: 9.75e1
variant carriers: 6194

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 18

GenotypeQuality
all individuals: 73
bin: 7.25e1
variant carriers: 10

GenotypeQuality
all individuals: 252
bin: 2.25e1
variant carriers: 81

GenotypeQuality
all individuals: 150
bin: 9.25e1
variant carriers: 33

European (Finnish)
type: Population
allele count: 816
allele frequency: 4.839857651245552e-1
allele num: 1686
num of homozygotes: 187

Other
type: Population
allele count: 93
allele frequency: 4.744897959183674e-1
allele num: 196
num of homozygotes: 22

Latino
type: Population
allele count: 117
allele frequency: 5.571428571428572e-1
allele num: 210
num of homozygotes: 37

East Asian
type: Population
allele count: 89
allele frequency: 4.405940594059406e-1
allele num: 202
num of homozygotes: 20

African
type: Population
allele count: 247
allele frequency: 3.199481865284974e-1
allele num: 772
num of homozygotes: 33

South Asian
type: Population
allele count: 4635
allele frequency: 6.084274087687057e-1
allele num: 7618
num of homozygotes: 1421

European (Non-Finnish)
type: Population
allele count: 2837
allele frequency: 5.796894156109522e-1
allele num: 4894
num of homozygotes: 810

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.797e0

QD
type: SiteQuality
SIO_000300: 2.983e1

DP
type: SiteQuality
SIO_000300: 3.69969e5

VQSLOD
type: SiteQuality
SIO_000300: 2.32e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 9.6e-2

FS
type: SiteQuality
SIO_000300: 3.182e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.109e-1

GenotypeQuality
all individuals: 126
bin: 6.75e1
variant carriers: 15

GenotypeQuality
all individuals: 6816
bin: 9.75e1
variant carriers: 6194

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 25

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 49

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 17

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 37

GenotypeQuality
all individuals: 100
bin: 1.25e1
variant carriers: 85

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 15

GenotypeQuality
all individuals: 258
bin: 2.25e1
variant carriers: 81

GenotypeQuality
all individuals: 73
bin: 7.25e1
variant carriers: 10

GenotypeQuality
all individuals: 118
bin: 7.75e1
variant carriers: 24

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 48

African
type: Population
allele count: 255
allele frequency: 3.244274809160305e-1
allele num: 786
num of homozygotes: 35

Other
type: Population
allele count: 92
allele frequency: 4.742268041237113e-1
allele num: 194
num of homozygotes: 22

European (Finnish)
type: Population
allele count: 824
allele frequency: 4.852767962308598e-1
allele num: 1698
num of homozygotes: 189

East Asian
type: Population
allele count: 94
allele frequency: 4.519230769230769e-1
allele num: 208
num of homozygotes: 22

European (Non-Finnish)
type: Population
allele count: 2875
allele frequency: 5.817482800485634e-1
allele num: 4942
num of homozygotes: 822

Latino
type: Population
allele count: 120
allele frequency: 5.555555555555556e-1
allele num: 216
num of homozygotes: 37

South Asian
type: Population
allele count: 4637
allele frequency: 6.086899448674192e-1
allele num: 7618
num of homozygotes: 1422

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

QD
type: SiteQuality
SIO_000300: 2.734e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e-1

FS
type: SiteQuality
SIO_000300: 2.983e0

VQSLOD
type: SiteQuality
SIO_000300: 3.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.124e-1

DP
type: SiteQuality
SIO_000300: 4.00846e5

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1733
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4886
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.564102564102564e-3
allele num: 780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1698
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.258e0

DP
type: SiteQuality
SIO_000300: 3.88464e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.618e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.871e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.38e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.72e-1

QD
type: SiteQuality
SIO_000300: 1.267e1

GenotypeQuality
all individuals: 96
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5385
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.044153720359771e-4
allele num: 4892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.35e-2

DP
type: SiteQuality
SIO_000300: 3.88552e5

QD
type: SiteQuality
SIO_000300: 1.404e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.075e0

FS
type: SiteQuality
SIO_000300: 2.105e0

MQRankSum
type: SiteQuality
SIO_000300: -1.157e0

VQSLOD
type: SiteQuality
SIO_000300: -9.647e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-2

MQ
type: SiteQuality
SIO_000300: 5.556e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

GenotypeQuality
all individuals: 171
bin: 8.25e1
variant carriers: 48

GenotypeQuality
all individuals: 131
bin: 7.75e1
variant carriers: 38

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 50

GenotypeQuality
all individuals: 137
bin: 6.75e1
variant carriers: 26

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 53

GenotypeQuality
all individuals: 889
bin: 7.5e0
variant carriers: 193

GenotypeQuality
all individuals: 172
bin: 9.25e1
variant carriers: 55

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 27

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 47

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 32

GenotypeQuality
all individuals: 97
bin: 7.25e1
variant carriers: 34

GenotypeQuality
all individuals: 213
bin: 6.25e1
variant carriers: 36

African
type: Population
allele count: 269
allele frequency: 3.135198135198135e-1
allele num: 858
num of homozygotes: 40

South Asian
type: Population
allele count: 4636
allele frequency: 6.087184873949579e-1
allele num: 7616
num of homozygotes: 1421

Latino
type: Population
allele count: 126
allele frequency: 5.526315789473685e-1
allele num: 228
num of homozygotes: 38

Other
type: Population
allele count: 94
allele frequency: 4.7e-1
allele num: 200
num of homozygotes: 22

East Asian
type: Population
allele count: 91
allele frequency: 4.504950495049505e-1
allele num: 202
num of homozygotes: 22

European (Non-Finnish)
type: Population
allele count: 2906
allele frequency: 5.814325730292117e-1
allele num: 4998
num of homozygotes: 847

European (Finnish)
type: Population
allele count: 844
allele frequency: 4.88991888760139e-1
allele num: 1726
num of homozygotes: 201

FS
type: SiteQuality
SIO_000300: 5.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.308e-1

QD
type: SiteQuality
SIO_000300: 2.184e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.48e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 6.05e0

DP
type: SiteQuality
SIO_000300: 4.17154e5

GenotypeQuality
all individuals: 1015
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6766
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 132
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.523977788995457e-4
allele num: 3962
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.223e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.87e-2

FS
type: SiteQuality
SIO_000300: 7.492e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.38e-1

DP
type: SiteQuality
SIO_000300: 5.32681e5

MQ
type: SiteQuality
SIO_000300: 5.876e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: -1.556e0

MQRankSum
type: SiteQuality
SIO_000300: -8.57e-1

GenotypeQuality
all individuals: 102
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2638
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6766
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3948
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 6.257822277847309e-4
allele num: 1598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.971e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.83e-2

QD
type: SiteQuality
SIO_000300: 1.388e1

MQRankSum
type: SiteQuality
SIO_000300: 5.15e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: -5.926e-1

FS
type: SiteQuality
SIO_000300: 3.043e0

DP
type: SiteQuality
SIO_000300: 5.32392e5

ClippingRankSum
type: SiteQuality
SIO_000300: -9.71e-1

GenotypeQuality
all individuals: 728
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 21

GenotypeQuality
all individuals: 46
bin: 6.25e1
variant carriers: 10

GenotypeQuality
all individuals: 41
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 50
bin: 8.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1948
bin: 7.5e0
variant carriers: 52

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 14

GenotypeQuality
all individuals: 6845
bin: 9.75e1
variant carriers: 1651

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 70
bin: 9.25e1
variant carriers: 7

GenotypeQuality
all individuals: 37
bin: 6.75e1
variant carriers: 15

East Asian
type: Population
allele count: 17
allele frequency: 8.415841584158416e-2
allele num: 202
num of homozygotes: 0

African
type: Population
allele count: 79
allele frequency: 1.400709219858156e-1
allele num: 564
num of homozygotes: 7

European (Non-Finnish)
type: Population
allele count: 415
allele frequency: 1.063012295081967e-1
allele num: 3904
num of homozygotes: 25

Latino
type: Population
allele count: 19
allele frequency: 1.01063829787234e-1
allele num: 188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 271
allele frequency: 1.697994987468672e-1
allele num: 1596
num of homozygotes: 24

Other
type: Population
allele count: 20
allele frequency: 1.08695652173913e-1
allele num: 184
num of homozygotes: 1

South Asian
type: Population
allele count: 947
allele frequency: 1.243108427408769e-1
allele num: 7618
num of homozygotes: 58

MQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.971e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.59e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 4.79e0

DP
type: SiteQuality
SIO_000300: 5.69261e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e-1

QD
type: SiteQuality
SIO_000300: 1.385e1

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

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 85
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6756
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1594
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.23e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 3.28e-1

QD
type: SiteQuality
SIO_000300: 2.018e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQ
type: SiteQuality
SIO_000300: 4.361e1

DP
type: SiteQuality
SIO_000300: 5.35995e5

GenotypeQuality
all individuals: 35
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2724
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1594
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312335958005249e-4
allele num: 7620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e0

DP
type: SiteQuality
SIO_000300: 5.35875e5

BaseQRankSum
type: SiteQuality
SIO_000300: -4.179e0

MQ
type: SiteQuality
SIO_000300: 5.837e1

VQSLOD
type: SiteQuality
SIO_000300: -2.822e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.32e-2

QD
type: SiteQuality
SIO_000300: 1.051e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e0

GenotypeQuality
all individuals: 69
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2736
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.361e1

QD
type: SiteQuality
SIO_000300: 8.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.33e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 4.15e-1

DP
type: SiteQuality
SIO_000300: 5.35846e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.231e0

GenotypeQuality
all individuals: 2746
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3896
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.026e0

DP
type: SiteQuality
SIO_000300: 5.35834e5

MQRankSum
type: SiteQuality
SIO_000300: -1.026e0

QD
type: SiteQuality
SIO_000300: 2.523e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.026e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: -1.426e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.712e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.35e-2

GenotypeQuality
all individuals: 291
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2677
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6757
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.026e0

QD
type: SiteQuality
SIO_000300: 2.524e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.35e-2

DP
type: SiteQuality
SIO_000300: 5.35682e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.026e0

MQ
type: SiteQuality
SIO_000300: 4.712e1

MQRankSum
type: SiteQuality
SIO_000300: -1.026e0

VQSLOD
type: SiteQuality
SIO_000300: 3.71e-1

GenotypeQuality
all individuals: 34
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2719
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6757
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.712e1

VQSLOD
type: SiteQuality
SIO_000300: -1.421e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 2.524e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.38e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.026e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.026e0

DP
type: SiteQuality
SIO_000300: 5.35722e5

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 7

GenotypeQuality
all individuals: 525
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.25e1
variant carriers: 23

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 17

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 74
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 6823
bin: 9.75e1
variant carriers: 1260

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.75e1
variant carriers: 32

GenotypeQuality
all individuals: 21
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 51
bin: 8.75e1
variant carriers: 5

African
type: Population
allele count: 46
allele frequency: 8.214285714285714e-2
allele num: 560
num of homozygotes: 2

Other
type: Population
allele count: 16
allele frequency: 8.695652173913043e-2
allele num: 184
num of homozygotes: 2

South Asian
type: Population
allele count: 480
allele frequency: 6.299212598425197e-2
allele num: 7620
num of homozygotes: 19

Latino
type: Population
allele count: 35
allele frequency: 1.861702127659574e-1
allele num: 188
num of homozygotes: 6

European (Finnish)
type: Population
allele count: 295
allele frequency: 1.848370927318296e-1
allele num: 1596
num of homozygotes: 28

European (Non-Finnish)
type: Population
allele count: 478
allele frequency: 1.223758320532514e-1
allele num: 3906
num of homozygotes: 43

East Asian
type: Population
allele count: 12
allele frequency: 5.94059405940594e-2
allele num: 202
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.162e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.820000000000001e-2

DP
type: SiteQuality
SIO_000300: 5.58423e5

QD
type: SiteQuality
SIO_000300: 1.475e1

GenotypeQuality
all individuals: 2414
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 63
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6732
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 54
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 80
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 6.281407035175879e-4
allele num: 1592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3902
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.59e-1

FS
type: SiteQuality
SIO_000300: 5.284e0

MQRankSum
type: SiteQuality
SIO_000300: 1.89e0

DP
type: SiteQuality
SIO_000300: 5.27192e5

MQ
type: SiteQuality
SIO_000300: 5.931e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.713e0

VQSLOD
type: SiteQuality
SIO_000300: -2.461e0

QD
type: SiteQuality
SIO_000300: 2.154e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.55e-2

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14537
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1412
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3937
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 137
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1762
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.310615989515072e-4
allele num: 7630
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1210
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6702
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.88e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.75e-1

DP
type: SiteQuality
SIO_000300: 5.19563e5

QD
type: SiteQuality
SIO_000300: 1.495e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

MQ
type: SiteQuality
SIO_000300: 5.821e1

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 554
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4224
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2054
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 8.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1782
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.47e-1

MQ
type: SiteQuality
SIO_000300: 5.682e1

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.340000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

DP
type: SiteQuality
SIO_000300: 5.584e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e-1

QD
type: SiteQuality
SIO_000300: 1.559e1

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

GenotypeQuality
all individuals: 313
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2409
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 111
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1581
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 195
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 9.75e1
variant carriers: 66

South Asian
type: Population
allele count: 67
allele frequency: 8.746736292428198e-3
allele num: 7660
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1784
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

FS
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.32e-2

DP
type: SiteQuality
SIO_000300: 5.6823e5

QD
type: SiteQuality
SIO_000300: 1.153e1

MQRankSum
type: SiteQuality
SIO_000300: 4.63e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

VQSLOD
type: SiteQuality
SIO_000300: -3.45e-2

GenotypeQuality
all individuals: 136
bin: 2.75e1
variant carriers: 20

GenotypeQuality
all individuals: 554
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2240
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 1.25e1
variant carriers: 11

GenotypeQuality
all individuals: 335
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2677
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 104
bin: 3.25e1
variant carriers: 17

GenotypeQuality
all individuals: 194
bin: 9.25e1
variant carriers: 6

GenotypeQuality
all individuals: 454
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 318
bin: 8.25e1
variant carriers: 6

South Asian
type: Population
allele count: 112
allele frequency: 1.460615545122587e-2
allele num: 7668
num of homozygotes: 1

Other
type: Population
allele count: 3
allele frequency: 1.31578947368421e-2
allele num: 228
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 1.767676767676768e-2
allele num: 396
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 7.2992700729927e-4
allele num: 1370
num of homozygotes: 0

East Asian
type: Population
allele count: 14
allele frequency: 2.845528455284553e-2
allele num: 492
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 4.435819240365955e-3
allele num: 7214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 39
allele frequency: 2.18609865470852e-2
allele num: 1784
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.80268e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.46e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.569999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.21e1

GenotypeQuality
all individuals: 3106
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 456
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 193
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1624
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.377031120903333e-4
allele num: 7262
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1786
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7674
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.74e0

MQ
type: SiteQuality
SIO_000300: 5.647e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.31e-2

DP
type: SiteQuality
SIO_000300: 5.78232e5

QD
type: SiteQuality
SIO_000300: 9.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e-1

GenotypeQuality
all individuals: 1260
bin: 6.75e1
variant carriers: 59

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 22

GenotypeQuality
all individuals: 17558
bin: 7.5e0
variant carriers: 131

GenotypeQuality
all individuals: 4315
bin: 2.25e1
variant carriers: 216

GenotypeQuality
all individuals: 982
bin: 1.75e1
variant carriers: 174

GenotypeQuality
all individuals: 600
bin: 2.75e1
variant carriers: 190

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 179

GenotypeQuality
all individuals: 3080
bin: 9.75e1
variant carriers: 2024

GenotypeQuality
all individuals: 530
bin: 7.75e1
variant carriers: 39

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 55

GenotypeQuality
all individuals: 219
bin: 5.75e1
variant carriers: 204

GenotypeQuality
all individuals: 399
bin: 8.25e1
variant carriers: 107

European (Non-Finnish)
type: Population
allele count: 1422
allele frequency: 1.539627544391511e-1
allele num: 9236
num of homozygotes: 61

African
type: Population
allele count: 51
allele frequency: 3.455284552845529e-2
allele num: 1476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 179
allele frequency: 9.401260504201681e-2
allele num: 1904
num of homozygotes: 7

Latino
type: Population
allele count: 50
allele frequency: 1.041666666666667e-1
allele num: 480
num of homozygotes: 0

Other
type: Population
allele count: 15
allele frequency: 6.35593220338983e-2
allele num: 236
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.291655902867476e-4
allele num: 7742
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.42045e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.623e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.57e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

MQ
type: SiteQuality
SIO_000300: 5.688e1

GenotypeQuality
all individuals: 595
bin: 8.25e1
variant carriers: 589

GenotypeQuality
all individuals: 1371
bin: 4.25e1
variant carriers: 1367

GenotypeQuality
all individuals: 545
bin: 5.25e1
variant carriers: 539

GenotypeQuality
all individuals: 622
bin: 4.75e1
variant carriers: 616

GenotypeQuality
all individuals: 4558
bin: 2.75e1
variant carriers: 4525

GenotypeQuality
all individuals: 3534
bin: 7.5e0
variant carriers: 2331

GenotypeQuality
all individuals: 2328
bin: 3.25e1
variant carriers: 2286

GenotypeQuality
all individuals: 14692
bin: 9.75e1
variant carriers: 14498

GenotypeQuality
all individuals: 400
bin: 5.75e1
variant carriers: 393

GenotypeQuality
all individuals: 395
bin: 6.25e1
variant carriers: 295

GenotypeQuality
all individuals: 5455
bin: 1.25e1
variant carriers: 5413

GenotypeQuality
all individuals: 6772
bin: 2.25e1
variant carriers: 5864

South Asian
type: Population
allele count: 9509
allele frequency: 8.918589382854999e-1
allele num: 10662
num of homozygotes: 4238

Latino
type: Population
allele count: 2382
allele frequency: 8.470839260312945e-1
allele num: 2812
num of homozygotes: 989

European (Finnish)
type: Population
allele count: 2882
allele frequency: 8.62874251497006e-1
allele num: 3340
num of homozygotes: 1243

European (Non-Finnish)
type: Population
allele count: 15415
allele frequency: 7.90350697292863e-1
allele num: 19504
num of homozygotes: 5949

African
type: Population
allele count: 2761
allele frequency: 7.402144772117962e-1
allele num: 3730
num of homozygotes: 977

East Asian
type: Population
allele count: 2946
allele frequency: 8.884197828709288e-1
allele num: 3316
num of homozygotes: 1301

Other
type: Population
allele count: 326
allele frequency: 8.402061855670103e-1
allele num: 388
num of homozygotes: 137

MQRankSum
type: SiteQuality
SIO_000300: -6.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.02e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.87388e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 3.277e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.963e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-2

MQ
type: SiteQuality
SIO_000300: 5.395e1

GenotypeQuality
all individuals: 4228
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1371
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4558
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3625
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14692
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 395
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2696
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3534
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.127153404429861e-5
allele num: 19504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3316
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3340
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.277e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.963e-1

MQ
type: SiteQuality
SIO_000300: 5.395e1

VQSLOD
type: SiteQuality
SIO_000300: 3.02e0

MQRankSum
type: SiteQuality
SIO_000300: -6.54e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.87388e5

GenotypeQuality
all individuals: 2662
bin: 4.25e1
variant carriers: 36

GenotypeQuality
all individuals: 4234
bin: 2.25e1
variant carriers: 22

GenotypeQuality
all individuals: 3628
bin: 4.75e1
variant carriers: 33

GenotypeQuality
all individuals: 3175
bin: 2.5e0
variant carriers: 16

GenotypeQuality
all individuals: 3769
bin: 3.75e1
variant carriers: 20

GenotypeQuality
all individuals: 1161
bin: 1.25e1
variant carriers: 18

GenotypeQuality
all individuals: 1951
bin: 5.75e1
variant carriers: 36

GenotypeQuality
all individuals: 3199
bin: 2.75e1
variant carriers: 23

GenotypeQuality
all individuals: 661
bin: 8.75e1
variant carriers: 30

GenotypeQuality
all individuals: 745
bin: 9.25e1
variant carriers: 33

GenotypeQuality
all individuals: 9996
bin: 6.25e1
variant carriers: 14

GenotypeQuality
all individuals: 3725
bin: 6.75e1
variant carriers: 34

South Asian
type: Population
allele count: 14
allele frequency: 9.005531969638492e-4
allele num: 15546
num of homozygotes: 0

Other
type: Population
allele count: 9
allele frequency: 1.308139534883721e-2
allele num: 688
num of homozygotes: 0

East Asian
type: Population
allele count: 55
allele frequency: 7.400430570505921e-3
allele num: 7432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 44
allele frequency: 8.593750000000001e-3
allele num: 5120
num of homozygotes: 0

African
type: Population
allele count: 93
allele frequency: 1.416387450502589e-2
allele num: 6566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 533
allele frequency: 1.031746031746032e-2
allele num: 51660
num of homozygotes: 0

Latino
type: Population
allele count: 25
allele frequency: 2.661839863713799e-3
allele num: 9392
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.350036e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

FS
type: SiteQuality
SIO_000300: 9.604900000000001e1

QD
type: SiteQuality
SIO_000300: 3.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.264e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.954e0

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

MQ
type: SiteQuality
SIO_000300: 5.8e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.86e-2

GenotypeQuality
all individuals: 5148
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3844
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2232
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13938
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2181
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3088
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2269
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7216
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.394964299135663e-5
allele num: 10644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55708
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.326259946949602e-3
allele num: 754
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7920
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

FS
type: SiteQuality
SIO_000300: 9.832000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

DP
type: SiteQuality
SIO_000300: 1.359637e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.447e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.65e-1

QD
type: SiteQuality
SIO_000300: 1.285e1

GenotypeQuality
all individuals: 5390
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3564
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3334
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15344
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4057
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variant carriers: 0

GenotypeQuality
all individuals: 3846
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 831
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2216
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5560
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.325110689437066e-5
allele num: 15810
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7918
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55774
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.64e-1

DP
type: SiteQuality
SIO_000300: 1.365268e6

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: 3.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 377
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2309
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3858
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 425
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18944
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1536
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5738
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.786799128042026e-5
allele num: 55966
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7948
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10668
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 1.39744e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.948e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 2.632e0

MQ
type: SiteQuality
SIO_000300: 6.194e1

QD
type: SiteQuality
SIO_000300: 2.195e1

GenotypeQuality
all individuals: 1454
bin: 7.5e0
variant carriers: 7

GenotypeQuality
all individuals: 707
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1761
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 971
bin: 1.25e1
variant carriers: 15

GenotypeQuality
all individuals: 2855
bin: 3.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1676
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1330
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1846
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1827
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1689
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 5454
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 3686
bin: 9.75e1
variant carriers: 8

African
type: Population
allele count: 3
allele frequency: 4.299226139294927e-4
allele num: 6978
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 5.141094481891923e-4
allele num: 52518
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.412429378531073e-3
allele num: 708
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.919877127863817e-4
allele num: 15626
num of homozygotes: 0

East Asian
type: Population
allele count: 13
allele frequency: 1.703800786369594e-3
allele num: 7630
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.241781548250265e-4
allele num: 9430
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.712e0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.839e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.04e-2

DP
type: SiteQuality
SIO_000300: 1.464076e6

FS
type: SiteQuality
SIO_000300: 6.1868e1

QD
type: SiteQuality
SIO_000300: 4.2e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.23e0

GenotypeQuality
all individuals: 864
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1038
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2447
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2791
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56834
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.249063202598052e-4
allele num: 8006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5738
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10790
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.481851e6

FS
type: SiteQuality
SIO_000300: 6.7285e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.218e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

VQSLOD
type: SiteQuality
SIO_000300: -2.311e1

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.482e0

MQ
type: SiteQuality
SIO_000300: 5.832e1

QD
type: SiteQuality
SIO_000300: 8.2e-1

GenotypeQuality
all individuals: 5950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2102
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2566
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 9.25e1
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GenotypeQuality
all individuals: 5078
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1835
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23098
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variant carriers: 0

GenotypeQuality
all individuals: 2321
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.75266404935502e-5
allele num: 57056
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5804
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.52e-1

MQ
type: SiteQuality
SIO_000300: 5.85e1

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.372e0

FS
type: SiteQuality
SIO_000300: 5.6193e1

QD
type: SiteQuality
SIO_000300: 8.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.663e1

DP
type: SiteQuality
SIO_000300: 1.506861e6

GenotypeQuality
all individuals: 324
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6671
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4368
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1055
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28620
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.690159889125511e-5
allele num: 59166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6046
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8140
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11030
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15954
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

FS
type: SiteQuality
SIO_000300: 4.866e0

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.676e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.64e-1

DP
type: SiteQuality
SIO_000300: 1.559115e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.55e0

QD
type: SiteQuality
SIO_000300: 1.861e1

GenotypeQuality
all individuals: 6648
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1050
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2014
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 221
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 166
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4721
bin: 9.75e1
variant carriers: 416

GenotypeQuality
all individuals: 28970
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2904
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 606
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1115
bin: 3.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 140
allele frequency: 2.361753095583522e-3
allele num: 59278
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 5.050505050505051e-3
allele num: 792
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15968
num of homozygotes: 0

African
type: Population
allele count: 207
allele frequency: 2.651127049180328e-2
allele num: 7808
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.649620587264929e-4
allele num: 6062
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.227295041728031e-4
allele num: 8148
num of homozygotes: 0

Latino
type: Population
allele count: 75
allele frequency: 6.787330316742082e-3
allele num: 11050
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

FS
type: SiteQuality
SIO_000300: 5.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.373e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

DP
type: SiteQuality
SIO_000300: 1.568132e6

GenotypeQuality
all individuals: 487
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2933
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2809
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3031
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4404
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6821
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.328783995206551e-5
allele num: 60082
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16018
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8218
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2429e1

MQRankSum
type: SiteQuality
SIO_000300: 4.07e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.702e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

QD
type: SiteQuality
SIO_000300: 1.109e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.315e0

MQ
type: SiteQuality
SIO_000300: 5.895e1

DP
type: SiteQuality
SIO_000300: 1.588169e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

GenotypeQuality
all individuals: 762
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2933
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3031
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4404
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2809
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.264542235710673e-4
allele num: 7908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.601024655779699e-4
allele num: 6246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8218
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.965393580778196e-5
allele num: 11154
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16018
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-2

FS
type: SiteQuality
SIO_000300: 1.2429e1

MQRankSum
type: SiteQuality
SIO_000300: 4.07e-1

QD
type: SiteQuality
SIO_000300: 1.109e1

DP
type: SiteQuality
SIO_000300: 1.588169e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 5.895e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.315e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.702e-1

GenotypeQuality
all individuals: 2823
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2808
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6849
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3062
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4412
bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60182
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.521432173474534e-4
allele num: 7932
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16028
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.21654501216545e-4
allele num: 8220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6264
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.14e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

VQSLOD
type: SiteQuality
SIO_000300: 4.74e-1

QD
type: SiteQuality
SIO_000300: 8.960000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

FS
type: SiteQuality
SIO_000300: 5.96e-1

DP
type: SiteQuality
SIO_000300: 1.592159e6

GenotypeQuality
all individuals: 1084
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3062
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6849
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4412
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 719
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30552
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7932
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.323252799840484e-5
allele num: 60182
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11160
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6264
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.14e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

QD
type: SiteQuality
SIO_000300: 8.960000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

DP
type: SiteQuality
SIO_000300: 1.592159e6

FS
type: SiteQuality
SIO_000300: 5.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

GenotypeQuality
all individuals: 639
bin: 7.25e1
variant carriers: 253

GenotypeQuality
all individuals: 243
bin: 3.75e1
variant carriers: 107

GenotypeQuality
all individuals: 580
bin: 9.25e1
variant carriers: 520

GenotypeQuality
all individuals: 33468
bin: 9.75e1
variant carriers: 33351

GenotypeQuality
all individuals: 2167
bin: 6.75e1
variant carriers: 384

GenotypeQuality
all individuals: 204
bin: 4.25e1
variant carriers: 107

GenotypeQuality
all individuals: 295
bin: 2.75e1
variant carriers: 55

GenotypeQuality
all individuals: 963
bin: 2.25e1
variant carriers: 55

GenotypeQuality
all individuals: 417
bin: 5.25e1
variant carriers: 278

GenotypeQuality
all individuals: 351
bin: 8.75e1
variant carriers: 303

GenotypeQuality
all individuals: 638
bin: 8.25e1
variant carriers: 497

GenotypeQuality
all individuals: 295
bin: 3.25e1
variant carriers: 100

GenotypeQuality
all individuals: 329
bin: 4.75e1
variant carriers: 208

South Asian
type: Population
allele count: 7552
allele frequency: 4.662303988146685e-1
allele num: 16198
num of homozygotes: 1805

European (Non-Finnish)
type: Population
allele count: 26532
allele frequency: 4.27907876911167e-1
allele num: 62004
num of homozygotes: 5747

Other
type: Population
allele count: 345
allele frequency: 4.116945107398568e-1
allele num: 838
num of homozygotes: 69

East Asian
type: Population
allele count: 3199
allele frequency: 3.826555023923445e-1
allele num: 8360
num of homozygotes: 626

African
type: Population
allele count: 1433
allele frequency: 1.75354870288791e-1
allele num: 8172
num of homozygotes: 118

Latino
type: Population
allele count: 6532
allele frequency: 5.744942832014072e-1
allele num: 11370
num of homozygotes: 1909

European (Finnish)
type: Population
allele count: 2083
allele frequency: 3.219474497681608e-1
allele num: 6470
num of homozygotes: 340

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

FS
type: SiteQuality
SIO_000300: 5.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.72e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

QD
type: SiteQuality
SIO_000300: 2.028e1

DP
type: SiteQuality
SIO_000300: 2.186156e6

GenotypeQuality
all individuals: 1243
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42345
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1315
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6358
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.606735434943282e-5
allele num: 62238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8184
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16186
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.699e0

QD
type: SiteQuality
SIO_000300: 1.442e1

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 1.3614e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.136e0

DP
type: SiteQuality
SIO_000300: 1.48716e6

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

GenotypeQuality
all individuals: 614
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6271
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.193032689095681e-4
allele num: 8382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.490832e6

MQ
type: SiteQuality
SIO_000300: 5.885e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 8.8e-1

QD
type: SiteQuality
SIO_000300: 1.238e1

VQSLOD
type: SiteQuality
SIO_000300: -2.952e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 301
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.604209445585216e-5
allele num: 62336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16184
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

DP
type: SiteQuality
SIO_000300: 1.491516e6

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.519e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

FS
type: SiteQuality
SIO_000300: 6.163e0

QD
type: SiteQuality
SIO_000300: 1.105e1

VQSLOD
type: SiteQuality
SIO_000300: -6.525e-1

GenotypeQuality
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bin: 4.25e1
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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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.179705846001731e-5
allele num: 16182
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.395e0

QD
type: SiteQuality
SIO_000300: 1.004e1

MQ
type: SiteQuality
SIO_000300: 5.89e1

DP
type: SiteQuality
SIO_000300: 1.494383e6

VQSLOD
type: SiteQuality
SIO_000300: -1.276e0

FS
type: SiteQuality
SIO_000300: 1.957e0

MQRankSum
type: SiteQuality
SIO_000300: -1.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.491e0

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.599334676774462e-5
allele num: 62526
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.61e0

MQRankSum
type: SiteQuality
SIO_000300: -9.89e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 1.499679e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
type: SiteQuality
SIO_000300: 1.452e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6229
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.354603249352484e-4
allele num: 8494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16174
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62912
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.434e0

DP
type: SiteQuality
SIO_000300: 1.514443e6

MQRankSum
type: SiteQuality
SIO_000300: 5.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

QD
type: SiteQuality
SIO_000300: 9.5e0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 593
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 2
allele frequency: 2.358490566037736e-4
allele num: 8480
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62926
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-2

FS
type: SiteQuality
SIO_000300: 2.007e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 1.218e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-1

DP
type: SiteQuality
SIO_000300: 1.514437e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 37
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62820
num of homozygotes: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.719207173194903e-4
allele num: 8476
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.183527083848628e-5
allele num: 16172
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.53e-1

QD
type: SiteQuality
SIO_000300: 1.274e1

MQ
type: SiteQuality
SIO_000300: 5.92e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.05e-1

DP
type: SiteQuality
SIO_000300: 1.515055e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.51e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.592204566442697e-5
allele num: 62806
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.514432e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.09e-1

FS
type: SiteQuality
SIO_000300: 2.334e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e0

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

QD
type: SiteQuality
SIO_000300: 1.001e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.596780889726312e-5
allele num: 62626
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.852e0

FS
type: SiteQuality
SIO_000300: 1.2492e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.50778e6

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.63e-1

MQ
type: SiteQuality
SIO_000300: 5.882e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-2

QD
type: SiteQuality
SIO_000300: 1.052e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.677e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 250
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GenotypeQuality
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GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.193561779452623e-5
allele num: 62626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.243e0

FS
type: SiteQuality
SIO_000300: 2.938e0

MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

MQ
type: SiteQuality
SIO_000300: 5.935e1

QD
type: SiteQuality
SIO_000300: 9.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.07e-1

DP
type: SiteQuality
SIO_000300: 1.507782e6

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 182
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.89521437466643e-5
allele num: 11242
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15956
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8050
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.554e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -5.014e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.553e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

DP
type: SiteQuality
SIO_000300: 1.48072e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.98e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10992
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.69606512890095e-5
allele num: 58960
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.899e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.31e-1

DP
type: SiteQuality
SIO_000300: 1.424516e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.241e1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 664
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 149
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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: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 579
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8020
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.458173392813916e-5
allele num: 57834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10892
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

DP
type: SiteQuality
SIO_000300: 1.398599e6

QD
type: SiteQuality
SIO_000300: 9.619999999999999e0

GenotypeQuality
all individuals: 486
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variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4176
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GenotypeQuality
all individuals: 233
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6046
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.992587574223887e-5
allele num: 50186
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14710
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

DP
type: SiteQuality
SIO_000300: 1.199011e6

QD
type: SiteQuality
SIO_000300: 1.622e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.912e0

MQ
type: SiteQuality
SIO_000300: 5.871e1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.48e-1

GenotypeQuality
all individuals: 1165
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16957
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4008
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GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.093350123898119e-5
allele num: 49234
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 5.630630630630631e-4
allele num: 7104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.3e-2

FS
type: SiteQuality
SIO_000300: 1.509e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.16e0

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-2

DP
type: SiteQuality
SIO_000300: 1.174815e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-1

QD
type: SiteQuality
SIO_000300: 1.784e1

GenotypeQuality
all individuals: 1525
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 878
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 160
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.183699458771092e-5
allele num: 31410
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4662
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.66994e5

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: 6.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.55e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-1

GenotypeQuality
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bin: 4.25e1
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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10738
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3014
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.066882853668423e-5
allele num: 19736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2760
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3430
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.19e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.179e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.37e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.97e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.96002e5

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2746
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.117206982543641e-4
allele num: 3208
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.383999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.84545e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.17e-2

FS
type: SiteQuality
SIO_000300: 6.292e0

QD
type: SiteQuality
SIO_000300: 7.83e0

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
all individuals: 2131
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variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18352
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.45000945000945e-5
allele num: 10582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2540
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.292e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.83e0

DP
type: SiteQuality
SIO_000300: 5.84545e5

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.17e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.383999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3810
bin: 6.25e1
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GenotypeQuality
all individuals: 71
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 516
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GenotypeQuality
all individuals: 561
bin: 9.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3248
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3208
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18352
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 6.292e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

QD
type: SiteQuality
SIO_000300: 7.83e0

VQSLOD
type: SiteQuality
SIO_000300: -7.383999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.17e-2

DP
type: SiteQuality
SIO_000300: 5.84545e5

GenotypeQuality
all individuals: 2124
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4797
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 211
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 356
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2708
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16160
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2272
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2972
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

VQSLOD
type: SiteQuality
SIO_000300: 3.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.88e-2

FS
type: SiteQuality
SIO_000300: 1.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.16e-1

DP
type: SiteQuality
SIO_000300: 5.51461e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.278e1

GenotypeQuality
all individuals: 2045
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3105
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4797
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16375
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 458
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16160
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2708
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.765625000000001e-5
allele num: 10240
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2972
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.36e0

FS
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.88e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.16e-1

DP
type: SiteQuality
SIO_000300: 5.51461e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 1.278e1