1-203766895-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203766895
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203766895
    reference: chr 1
allele count: 32
allele frequency: 2.755769893213917e-3
allele num: 11612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1271C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1271C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1166C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+1973C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.245C>T
  hgvsp: ENSP00000447879.1:p.Ala82Val
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1271C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+1973C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1166C>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala82Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

1-203766919-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203766919
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203766919
    reference: chr 1
allele count: 1
allele frequency: 8.571918395336877e-5
allele num: 11666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1295G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1295G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+1997G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1190G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1190G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+1997G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.269G>A
  hgvsp: ENSP00000447879.1:p.Gly90Glu
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1295G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1738
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly90Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ

1-203766921-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203766921
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203766921
    reference: chr 1
allele count: 1
allele frequency: 8.566044200788077e-5
allele num: 11674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1297T>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+1999T>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1297T>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1297T>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1192T>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+1999T>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.271T>A
  hgvsp: ENSP00000447879.1:p.Ser91Thr
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1192T>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3211
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser91Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

1-203766964-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203766964
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203766964
    reference: chr 1
allele count: 554
allele frequency: 4.644533869885983e-2
allele num: 11928
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.314A>G
  hgvsp: ENSP00000447879.1:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2042A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1340A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1340A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2042A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1235A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1235A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1340A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 2.5e0
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 2.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.5e0
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3165
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 7.5e0
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asn105Ser
num of homozygotes: 23
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/1-203766990-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203766990
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203766990
    reference: chr 1
allele count: 1
allele frequency: 8.264462809917356e-5
allele num: 12100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1366C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2068C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2068C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.340C>A
  hgvsp: ENSP00000447879.1:p.Leu114Ile
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1261C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1366C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1366C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1261C>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu114Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-203767005-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767005
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767005
    reference: chr 1
allele count: 2
allele frequency: 1.645007402533311e-4
allele num: 12158
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.355A>G
  hgvsp: ENSP00000447879.1:p.Ile119Val
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2083A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1276A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1276A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2083A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1381A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1381A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1381A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3598
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile119Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

1-203767019-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767019
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767019
    reference: chr 1
allele count: 7
allele frequency: 5.733005733005733e-4
allele num: 12210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1395C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1290C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2097C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.369C>T
  hgvsp: ENST00000550078.1:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1395C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1290C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2097C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1395C>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3618
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile123Ile
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

1-203767130-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767130
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767130
    reference: chr 1
allele count: 1
allele frequency: 8.115565654926148e-5
allele num: 12322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1506G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2208G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1401G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.480G>A
  hgvsp: ENST00000550078.1:c.480G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2208G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1401G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1506G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1506G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg160Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

1-203767165-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767165
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767165
    reference: chr 1
allele count: 1
allele frequency: 8.111615833874107e-5
allele num: 12328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1541T>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1436T>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1541T>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2243T>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.515T>A
  hgvsp: ENSP00000447879.1:p.Leu172His
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2243T>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1541T>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1436T>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3814
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu172His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

1-203767169-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767169
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767169
    reference: chr 1
allele count: 1
allele frequency: 8.110300081103001e-5
allele num: 12330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2247A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1545A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.519A>G
  hgvsp: ENST00000550078.1:c.519A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1545A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1440A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1440A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2247A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1545A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3813
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln173Gln
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

1-203767220-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767220
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767220
    reference: chr 1
allele count: 2
allele frequency: 1.622323166774821e-4
allele num: 12328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2298T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2298T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1491T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1596T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1491T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1596T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.570T>G
  hgvsp: ENSP00000447879.1:p.Phe190Leu
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1596T>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe190Leu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

1-203767230-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767230
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767230
    reference: chr 1
allele count: 8
allele frequency: 6.490345610903781e-4
allele num: 12326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1501A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2308A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1606A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.580A>G
  hgvsp: ENSP00000447879.1:p.Ser194Gly
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1501A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1606A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1606A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2308A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser194Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum

1-203767235-AGAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767235
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767232
    reference: chr 1
allele count: 2
allele frequency: 1.622586402725945e-4
allele num: 12326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1617_345+1619delGGA
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2319_135+2321delGGA
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.591_593delGGA
  hgvsp: ENSP00000447879.1:p.Glu197del
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2319_-206+2321delGGA
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1617_-260+1619delGGA
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1512_-260+1514delGGA
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1512_-565+1514delGGA
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1617_-565+1619delGGA
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu197del
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: AGAG
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

1-203767241-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767241
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767241
    reference: chr 1
allele count: 1
allele frequency: 8.114248620577734e-5
allele num: 12324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2319G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1617G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.591G>A
  hgvsp: ENST00000550078.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1512G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1512G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1617G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2319G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1617G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu197Glu
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ

1-203767250-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767250
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767250
    reference: chr 1
allele count: 7
allele frequency: 5.680895958448304e-4
allele num: 12322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2328C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1626C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2328C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1626C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.600C>T
  hgvsp: ENST00000550078.1:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1521C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1521C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1626C>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3807
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr200Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD

1-203767283-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767283
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767283
    reference: chr 1
allele count: 2
allele frequency: 1.62311313098523e-4
allele num: 12322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2361C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1554C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1659C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1554C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1659C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1659C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.633C>G
  hgvsp: ENSP00000447879.1:p.Ser211Arg
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2361C>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3843
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1586
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser211Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP

1-203767285-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767285
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767285
    reference: chr 1
allele count: 1
allele frequency: 8.115565654926148e-5
allele num: 12322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1661A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.635A>G
  hgvsp: ENSP00000447879.1:p.Asn212Ser
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2363A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1556A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1556A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2363A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1661A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1661A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn212Ser
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

1-203767328-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767328
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767328
    reference: chr 1
allele count: 1
allele frequency: 8.118201006656925e-5
allele num: 12318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1704T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1599T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1599T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1704T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.678T>C
  hgvsp: ENST00000550078.1:c.678T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2406T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2406T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1704T>C
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3842
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn226Asn
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

1-203767353-TCAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767353
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767350
    reference: chr 1
allele count: 1
allele frequency: 8.118201006656925e-5
allele num: 12318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1627_-260+1629delGCA
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1732_345+1734delGCA
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2434_-206+2436delGCA
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1732_-565+1734delGCA
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1627_-565+1629delGCA
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.706_708delGCA
  hgvsp: ENSP00000447879.1:p.Ala236del
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2434_135+2436delGCA
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1732_-260+1734delGCA
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3824
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1556
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala236del
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: TCAG
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

1-203767374-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767374
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767374
    reference: chr 1
allele count: 3
allele frequency: 2.436251421146662e-4
allele num: 12314
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.724G>C
  hgvsp: ENSP00000447879.1:p.Ala242Pro
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2452G>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1645G>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1750G>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1750G>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1750G>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1645G>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2452G>C
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala242Pro
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

1-203767375-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767375
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767375
    reference: chr 1
allele count: 1
allele frequency: 8.122157244964262e-5
allele num: 12312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1751C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2453C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1751C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2453C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1646C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.725C>T
  hgvsp: ENSP00000447879.1:p.Ala242Val
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1751C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1646C>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala242Val
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

1-203767387-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767387
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767387
    reference: chr 1
allele count: 1
allele frequency: 8.118201006656925e-5
allele num: 12318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1763G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2465G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.737G>A
  hgvsp: ENSP00000447879.1:p.Arg246Lys
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1658G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1763G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2465G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1658G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1763G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg246Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD

1-203767394-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767394
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767394
    reference: chr 1
allele count: 1
allele frequency: 8.119519324455992e-5
allele num: 12316
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.744C>T
  hgvsp: ENST00000550078.1:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1665C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2472C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1770C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2472C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1665C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1770C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1770C>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu248Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

1-203767442-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767442
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767442
    reference: chr 1
allele count: 1
allele frequency: 8.116883116883117e-5
allele num: 12320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1818C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2520C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1818C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2520C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1818C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1713C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.792C>G
  hgvsp: ENST00000550078.1:c.792C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1713C>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3835
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1497
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala264Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

1-203767520-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767520
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767520
    reference: chr 1
allele count: 1
allele frequency: 8.171269815329302e-5
allele num: 12238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1791A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.870A>G
  hgvsp: ENST00000550078.1:c.870A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1896A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1896A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2598A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1896A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2598A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1791A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3554
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg290Arg
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

1-203767531-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767531
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767531
    reference: chr 1
allele count: 1
allele frequency: 8.183306055646482e-5
allele num: 12220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1802G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1907G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.881G>A
  hgvsp: ENSP00000447879.1:p.Arg294Gln
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1802G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2609G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2609G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1907G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1907G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3459
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg294Gln
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-203767563-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767563
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767563
    reference: chr 1
allele count: 1
allele frequency: 8.21962847279303e-5
allele num: 12166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1939A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1939A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1834A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1834A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2641A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2641A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1939A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.913A>G
  hgvsp: ENSP00000447879.1:p.Thr305Ala
  variant of: http://identifiers.org/hgnc/33273
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr305Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

1-203767571-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767571
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767571
    reference: chr 1
allele count: 2
allele frequency: 1.64446637066272e-4
allele num: 12162
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1947A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2649A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1947A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2649A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1947A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.921A>G
  hgvsp: ENST00000550078.1:c.921A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1842A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1842A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln307Gln
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

1-203767596-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767596
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767596
    reference: chr 1
allele count: 6
allele frequency: 4.93421052631579e-4
allele num: 12160
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1972A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1867A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1972A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1972A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2674A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1867A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.946A>G
  hgvsp: ENSP00000447879.1:p.Ile316Val
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2674A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile316Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

1-203767601-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767601
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767601
    reference: chr 1
allele count: 2
allele frequency: 1.643655489809336e-4
allele num: 12168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2679T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.951T>C
  hgvsp: ENST00000550078.1:c.951T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1872T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1977T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2679T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1977T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1872T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1977T>C
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 7.75e1
  variant carriers: 0
hgvs: p.His317His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

1-203767620-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767620
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767620
    reference: chr 1
allele count: 1
allele frequency: 8.21422704123542e-5
allele num: 12174
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.970G>A
  hgvsp: ENSP00000447879.1:p.Asp324Asn
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2698G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+1996G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+1996G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+1996G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2698G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1891G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1891G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3510
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp324Asn
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

1-203767624-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767624
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767624
    reference: chr 1
allele count: 26
allele frequency: 2.136400986031224e-3
allele num: 12170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2702G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2702G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.974G>A
  hgvsp: ENSP00000447879.1:p.Ser325Asn
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2000G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1895G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2000G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1895G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2000G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser325Asn
num of homozygotes: 2
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

1-203767674-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767674
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767674
    reference: chr 1
allele count: 2
allele frequency: 1.642036124794746e-4
allele num: 12180
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1024C>T
  hgvsp: ENSP00000447879.1:p.Leu342Phe
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2050C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1945C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2752C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2050C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1945C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2050C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2752C>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3563
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu342Phe
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

1-203767701-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767701
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767701
    reference: chr 1
allele count: 1
allele frequency: 8.208832703989493e-5
allele num: 12182
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1051A>G
  hgvsp: ENSP00000447879.1:p.Lys351Glu
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2077A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1972A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1972A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2077A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2779A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2779A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2077A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3496
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys351Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

1-203767702-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767702
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767702
    reference: chr 1
allele count: 1
allele frequency: 8.210180623973728e-5
allele num: 12180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2780A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2078A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2780A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2078A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1973A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1052A>G
  hgvsp: ENSP00000447879.1:p.Lys351Arg
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2078A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1973A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1773
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys351Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-203767726-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767726
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767726
    reference: chr 1
allele count: 1
allele frequency: 8.21422704123542e-5
allele num: 12174
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2804C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2804C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1076C>G
  hgvsp: ENSP00000447879.1:p.Thr359Arg
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2102C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+1997C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2102C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2102C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+1997C>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3398
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1653
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr359Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

1-203767763-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767763
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767763
    reference: chr 1
allele count: 1
allele frequency: 8.18464560484531e-5
allele num: 12218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2841T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2034T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1113T>G
  hgvsp: ENST00000550078.1:c.1113T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2139T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2034T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2139T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2841T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2139T>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1772
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro371Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

1-203767773-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767773
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767773
    reference: chr 1
allele count: 1
allele frequency: 8.175277959450622e-5
allele num: 12232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2044G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2851G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2149G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1123G>T
  hgvsp: ENSP00000447879.1:p.Val375Phe
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2851G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2149G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2044G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2149G>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3533
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1740
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val375Phe
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

1-203767803-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767803
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767803
    reference: chr 1
allele count: 3
allele frequency: 2.444589308996089e-4
allele num: 12272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2881G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2179G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2074G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2074G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1153G>A
  hgvsp: ENSP00000447879.1:p.Val385Ile
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.135+2881G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2179G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2179G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val385Ile
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-203767822-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767822
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767822
    reference: chr 1
allele count: 1236
allele frequency: 1.003409644422796e-1
allele num: 12318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2198T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2881T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2198T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2198T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1172T>G
  hgvsp: ENSP00000447879.1:p.Leu391Arg
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2093T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2900T>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2093T>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 3.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 2.5e0
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 2.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 71
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 3270
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 7.5e0
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 9.25e1
  variant carriers: 4
hgvs: p.Leu391Arg
num of homozygotes: 63
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

1-203767832-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767832
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767832
    reference: chr 1
allele count: 2
allele frequency: 1.623376623376623e-4
allele num: 12320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2103G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1182G>A
  hgvsp: ENST00000550078.1:c.1182G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2208G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2208G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2871G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2910G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2208G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2103G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala394Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

1-203767833-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767833
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767833
    reference: chr 1
allele count: 1
allele frequency: 8.116883116883117e-5
allele num: 12320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2209C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2209C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2870C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1183C>T
  hgvsp: ENSP00000447879.1:p.Gln395Ter
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2209C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2104C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2104C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2911C>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln395Ter
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

1-203767850-ATGT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767850
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767847
    reference: chr 1
allele count: 1
allele frequency: 8.115565654926148e-5
allele num: 12322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2230_345+2232delTGT
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2849_136-2847delTGT
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2932_-206+2934delTGT
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2230_-260+2232delTGT
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2125_-260+2127delTGT
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1204_1206delTGT
  hgvsp: ENSP00000447879.1:p.Cys402del
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2125_-565+2127delTGT
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2230_-565+2232delTGT
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Cys402del
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: ATGT
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

1-203767880-AAGTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767880
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767876
    reference: chr 1
allele count: 1
allele frequency: 8.116883116883117e-5
allele num: 12320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2259_-565+2262delTCAG
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2820_136-2817delTCAG
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2961_-206+2964delTCAG
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2259_345+2262delTCAG
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2154_-565+2157delTCAG
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2259_-260+2262delTCAG
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1233_1236delTCAG
  hgvsp: ENSP00000447879.1:p.Ser411ArgfsTer6
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2154_-260+2157delTCAG
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1769
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3934
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser411ArgfsTer6
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: AAGTC
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

1-203767890-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767890
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767890
    reference: chr 1
allele count: 1
allele frequency: 8.116883116883117e-5
allele num: 12320
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1240A>G
  hgvsp: ENSP00000447879.1:p.Ile414Val
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2161A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2266A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2161A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2266A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2813A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2266A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+2968A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1767
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile414Val
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

1-203767926-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767926
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767926
    reference: chr 1
allele count: 1
allele frequency: 8.120838070488874e-5
allele num: 12314
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1276A>G
  hgvsp: ENSP00000447879.1:p.Asn426Asp
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2197A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2302A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2197A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2302A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3004A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2777A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2302A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn426Asp
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

1-203767930-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767930
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767930
    reference: chr 1
allele count: 1
allele frequency: 8.120838070488874e-5
allele num: 12314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2306A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2306A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2201A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2306A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3008A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2201A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2773A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1280A>G
  hgvsp: ENSP00000447879.1:p.Tyr427Cys
  variant of: http://identifiers.org/hgnc/33273
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr427Cys
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

1-203767943-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203767943
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203767943
    reference: chr 1
allele count: 6
allele frequency: 4.872502842293325e-4
allele num: 12314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2760A>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2214A>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2319A>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2319A>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2319A>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1293A>T
  hgvsp: ENST00000550078.1:c.1293A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3021A>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2214A>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3897
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro431Pro
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

1-203768021-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768021
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768021
    reference: chr 1
allele count: 12
allele frequency: 9.745005684586649e-4
allele num: 12314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2292A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2397A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2292A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-4269A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1371A>G
  hgvsp: ENST00000550078.1:c.1371A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2682A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3099A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2397A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2397A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1421
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3925
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val457Val
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS

1-203768062-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768062
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768062
    reference: chr 1
allele count: 1
allele frequency: 8.123476848090982e-5
allele num: 12310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2333C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2438C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3140C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2438C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-4228C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1412C>T
  hgvsp: ENSP00000447879.1:p.Thr471Ile
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2333C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2438C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2641C>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3861
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr471Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

1-203768077-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768077
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768077
    reference: chr 1
allele count: 1
allele frequency: 8.120838070488874e-5
allele num: 12314
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1427A>G
  hgvsp: ENSP00000447879.1:p.Gln476Arg
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2348A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-4213A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2453A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2453A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2626A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3155A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2348A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2453A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln476Arg
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

1-203768116-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768116
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768116
    reference: chr 1
allele count: 1
allele frequency: 8.123476848090982e-5
allele num: 12310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3194A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-565+2492A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2587A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2387A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1466A>G
  hgvsp: ENSP00000447879.1:p.His489Arg
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-260+2492A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2387A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.345+2492A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-4174A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3824
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His489Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

1-203768173-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768173
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768173
    reference: chr 1
allele count: 8
allele frequency: 6.501950585175553e-4
allele num: 12304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2444C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2530C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1523C>T
  hgvsp: ENSP00000447879.1:p.Ala508Val
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2530C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2530C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2444C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3251C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-4117C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2530C>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3845
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 9.75e1
  variant carriers: 8
hgvs: p.Ala508Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-203768174-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768174
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768174
    reference: chr 1
allele count: 1
allele frequency: 8.126117341134406e-5
allele num: 12306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3252G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2529G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-4116G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2445G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1524G>A
  hgvsp: ENST00000550078.1:c.1524G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2529G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2529G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2445G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2529G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala508Ala
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/1-203768200-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768200
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768200
    reference: chr 1
allele count: 1
allele frequency: 8.127438231469441e-5
allele num: 12304
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1550C>A
  hgvsp: ENSP00000447879.1:p.Pro517His
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2503C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-4090C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3278C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2503C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2503C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2503C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2471C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2471C>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro517His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

1-203768201-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768201
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768201
    reference: chr 1
allele count: 2
allele frequency: 1.625223468226881e-4
allele num: 12306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-4089C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2502C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2502C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2472C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3279C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2472C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1551C>T
  hgvsp: ENST00000550078.1:c.1551C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2502C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2502C>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro517Pro
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

1-203768202-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768202
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768202
    reference: chr 1
allele count: 6
allele frequency: 4.877255730775484e-4
allele num: 12302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-4088G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3280G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2501G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-260+2473G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1552G>A
  hgvsp: ENSP00000447879.1:p.Asp518Asn
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2501G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-565+2473G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2501G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2501G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3898
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp518Asn
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ

1-203768297-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768297
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768297
    reference: chr 1
allele count: 1
allele frequency: 8.141996417521577e-5
allele num: 12282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2406G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1647G>A
  hgvsp: ENST00000550078.1:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2406G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2406G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2406G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2406G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2406G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3993G>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3375G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu549Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

1-203768328-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768328
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768328
    reference: chr 1
allele count: 2010
allele frequency: 1.636541279921837e-1
allele num: 12282
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1678T>C
  hgvsp: ENSP00000447879.1:p.Phe560Leu
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3406T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2375T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2375T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2375T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2375T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2375T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3962T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2375T>C
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 2.5e0
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 176
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 182
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.25e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 2.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 188
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 2.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 165
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3084
  bin: 6.25e1
  variant carriers: 8
hgvs: p.Phe560Leu
num of homozygotes: 190
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

1-203768338-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768338
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768338
    reference: chr 1
allele count: 9
allele frequency: 7.321835340058575e-4
allele num: 12292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2365C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3416C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2365C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2365C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2365C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2365C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1688C>G
  hgvsp: ENSP00000447879.1:p.Ser563Cys
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3952C>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2365C>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3902
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser563Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/1-203768342-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768342
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768342
    reference: chr 1
allele count: 10
allele frequency: 8.132726089785296e-4
allele num: 12296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2361C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1692C>A
  hgvsp: ENSP00000447879.1:p.Asp564Glu
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2361C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2361C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2361C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2361C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3948C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3420C>A
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2361C>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1621
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp564Glu
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

1-203768362-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768362
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768362
    reference: chr 1
allele count: 1
allele frequency: 8.132726089785297e-5
allele num: 12296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3440A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2341A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2341A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2341A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3928A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2341A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2341A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1712A>G
  hgvsp: ENSP00000447879.1:p.His571Arg
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2341A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His571Arg
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

1-203768371-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768371
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768371
    reference: chr 1
allele count: 38
allele frequency: 3.089430894308943e-3
allele num: 12300
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1721A>G
  hgvsp: ENSP00000447879.1:p.Lys574Arg
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2332A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2332A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3919A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2332A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2332A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3449A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2332A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2332A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys574Arg
num of homozygotes: 1
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

1-203768378-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768378
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768378
    reference: chr 1
allele count: 5
allele frequency: 4.065040650406504e-4
allele num: 12300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2325T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2325T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1728T>C
  hgvsp: ENST00000550078.1:c.1728T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3456T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2325T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2325T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2325T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3912T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2325T>C
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly576Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: T
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

1-203768432-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768432
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768432
    reference: chr 1
allele count: 1
allele frequency: 8.126117341134406e-5
allele num: 12306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3858C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2271C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3510C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1782C>T
  hgvsp: ENST00000550078.1:c.1782C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2271C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2271C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2271C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2271C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2271C>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4021
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp594Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

1-203768435-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768435
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768435
    reference: chr 1
allele count: 38
allele frequency: 3.087924589631074e-3
allele num: 12306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2268T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2268T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2268T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1785T>C
  hgvsp: ENST00000550078.1:c.1785T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3513T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2268T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2268T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3855T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2268T>C
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe595Phe
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

1-203768441-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768441
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768441
    reference: chr 1
allele count: 1
allele frequency: 8.127438231469441e-5
allele num: 12304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3519C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1791C>T
  hgvsp: ENST00000550078.1:c.1791C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3849C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2262C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2262C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2262C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2262C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2262C>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2262C>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4021
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Cys597Cys
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum

1-203768442-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768442
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768442
    reference: chr 1
allele count: 1
allele frequency: 8.127438231469441e-5
allele num: 12304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2261G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3848G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2261G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2261G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2261G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2261G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1792G>T
  hgvsp: ENSP00000447879.1:p.Glu598Ter
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2261G>T
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3520G>T
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu598Ter
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum

1-203768461-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768461
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768461
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 12308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2242A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2242A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3829A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2242A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2242A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1811A>G
  hgvsp: ENSP00000447879.1:p.Asn604Ser
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2242A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2242A>G
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3539A>G
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4050
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn604Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

1-203768486-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768486
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768486
    reference: chr 1
allele count: 1
allele frequency: 8.120838070488874e-5
allele num: 12314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356181
  ensembl transcript: ENST00000367212
  gene symbol: ZC3H11A
  hgvsc: ENST00000367212.3:c.-259-2217T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000406531
  ensembl transcript: ENST00000432282
  gene symbol: ZC3H11A
  hgvsc: ENST00000432282.1:c.-259-2217T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257315
  ensembl protein: ENSP00000447879
  ensembl transcript: ENST00000550078
  gene symbol: ZBED6
  hgvsc: ENST00000550078.1:c.1836T>C
  hgvsp: ENST00000550078.1:c.1836T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33273
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000466470
  gene symbol: ZC3H11A
  hgvsc: ENST00000466470.1:n.346-2217T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000438527
  ensembl transcript: ENST00000545588
  gene symbol: ZC3H11A
  hgvsc: ENST00000545588.1:c.-3804T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000356183
  ensembl transcript: ENST00000367214
  gene symbol: ZC3H11A
  hgvsc: ENST00000367214.1:c.-564-2217T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000333253
  ensembl transcript: ENST00000332127
  gene symbol: ZC3H11A
  hgvsc: ENST00000332127.4:c.-564-2217T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000415072
  ensembl transcript: ENST00000453771
  gene symbol: ZC3H11A
  hgvsc: ENST00000453771.1:c.-206+3564T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000058673
  ensembl protein: ENSP00000432602
  ensembl transcript: ENST00000495527
  gene symbol: ZC3H11A
  hgvsc: ENST00000495527.1:c.-3804T>C
  variant of: http://identifiers.org/hgnc/29093
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2217T>C
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr612Thr
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

1-203768508-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 203768508
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 203768508
    reference: chr 1
allele count: 1
allele frequency: 8.122157244964262e-5
allele num: 12312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058673
  ensembl transcript: ENST00000461980
  gene symbol: ZC3H11A
  hgvsc: ENST00000461980.1:n.136-2195G>A
  variant of: http://identifiers.org/hgnc/29093
canonical: true
consequence: missense
filter: PASS
hgvs: p.Val620Ile
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 376
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3116
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 9.75e1
variant carriers: 33

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 1

African
type: Population
allele count: 2
allele frequency: 5.181347150259068e-3
allele num: 386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 7.042253521126761e-3
allele num: 142
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 8.369497830130192e-3
allele num: 3226
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.646202699126753e-4
allele num: 7558
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.42e0

MQRankSum
type: SiteQuality
SIO_000300: 1.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.295e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.34e1

DP
type: SiteQuality
SIO_000300: 1.7282e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.52e-2

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

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 317
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3197
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.5e-3
allele num: 400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7562
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.71e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.669999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

QD
type: SiteQuality
SIO_000300: 1.092e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.616e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.08e-1

FS
type: SiteQuality
SIO_000300: 1.935e0

DP
type: SiteQuality
SIO_000300: 1.7315e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 216
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 743
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.322751322751323e-4
allele num: 7560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3260
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

FS
type: SiteQuality
SIO_000300: 1.388e1

VQSLOD
type: SiteQuality
SIO_000300: -1.734e0

DP
type: SiteQuality
SIO_000300: 1.73355e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 1.339e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.72e-2

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.51e-1

GenotypeQuality
all individuals: 710
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 7

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 864
bin: 9.75e1
variant carriers: 524

GenotypeQuality
all individuals: 300
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 135
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 288
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 119
bin: 8.75e1
variant carriers: 3

Other
type: Population
allele count: 5
allele frequency: 3.90625e-2
allele num: 128
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 3.614457831325301e-2
allele num: 166
num of homozygotes: 0

East Asian
type: Population
allele count: 57
allele frequency: 3.031914893617021e-1
allele num: 188
num of homozygotes: 6

South Asian
type: Population
allele count: 351
allele frequency: 4.629385386441572e-2
allele num: 7582
num of homozygotes: 10

African
type: Population
allele count: 74
allele frequency: 1.516393442622951e-1
allele num: 488
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 61
allele frequency: 1.806872037914692e-2
allele num: 3376
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.26e-2

DP
type: SiteQuality
SIO_000300: 2.06481e5

QD
type: SiteQuality
SIO_000300: 1.23e1

GenotypeQuality
all individuals: 169
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 207
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3561
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.315443304393581e-4
allele num: 7602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3498
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.93e0

DP
type: SiteQuality
SIO_000300: 1.76934e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.55e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.186e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: -2.246e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-2

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

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

GenotypeQuality
all individuals: 200
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.630886608787161e-4
allele num: 7602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3538
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.49e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

DP
type: SiteQuality
SIO_000300: 1.77536e5

FS
type: SiteQuality
SIO_000300: 3.257e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.18e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.14e1

GenotypeQuality
all individuals: 1526
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 9.200841219768665e-4
allele num: 7608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3566
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.78101e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.56e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e-1

FS
type: SiteQuality
SIO_000300: 2.587e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.675e0

MQRankSum
type: SiteQuality
SIO_000300: 5.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

QD
type: SiteQuality
SIO_000300: 1.357e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1792
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3814
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 344
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 316
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.759381898454746e-4
allele num: 3624
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: 558
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: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.131e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.171e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.26e-1

DP
type: SiteQuality
SIO_000300: 1.80587e5

QD
type: SiteQuality
SIO_000300: 1.492e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.68e-2

MQ
type: SiteQuality
SIO_000300: 5.949e1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e0

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

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1895
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 826
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 376
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
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: 0
allele frequency: 0.0e0
allele num: 2
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: 1
allele frequency: 5.050505050505051e-3
allele num: 198
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: 132
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

QD
type: SiteQuality
SIO_000300: 1.197e1

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

DP
type: SiteQuality
SIO_000300: 1.81042e5

FS
type: SiteQuality
SIO_000300: 4.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.94e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.53e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

VQSLOD
type: SiteQuality
SIO_000300: -2.299e0

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

GenotypeQuality
all individuals: 82
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 194
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 345
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.76678445229682e-3
allele num: 566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
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: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
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: 198
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.01e-1

MQ
type: SiteQuality
SIO_000300: 5.398e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: -9.595e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.97e-2

FS
type: SiteQuality
SIO_000300: 2.522e0

DP
type: SiteQuality
SIO_000300: 1.81057e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e0

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3797
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1948
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 375
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 206
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 3.53356890459364e-3
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: 132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3622
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: 2.357e0

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.9e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.80986e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.06e-2

QD
type: SiteQuality
SIO_000300: 1.296e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

GenotypeQuality
all individuals: 341
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3785
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 313
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
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: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3622
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 1.418439716312057e-2
allele num: 564
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.97e0

FS
type: SiteQuality
SIO_000300: 5.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.65e-2

QD
type: SiteQuality
SIO_000300: 1.391e1

DP
type: SiteQuality
SIO_000300: 1.80873e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3790
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1862
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 9.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
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: 132
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.759381898454746e-4
allele num: 3624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.80515e5

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

MQRankSum
type: SiteQuality
SIO_000300: -1.145e0

FS
type: SiteQuality
SIO_000300: 4.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.79e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.28e-1

MQ
type: SiteQuality
SIO_000300: 5.78e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.89e-1

QD
type: SiteQuality
SIO_000300: 1.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3796
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
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: 1
allele frequency: 1.312335958005249e-4
allele num: 7620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.77e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.389e0

DP
type: SiteQuality
SIO_000300: 1.80218e5

MQRankSum
type: SiteQuality
SIO_000300: 9.03e-1

FS
type: SiteQuality
SIO_000300: 3.287e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 202
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 149
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1720
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 9.186351706036745e-4
allele num: 7620
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.447e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

FS
type: SiteQuality
SIO_000300: 5.873e0

DP
type: SiteQuality
SIO_000300: 1.79996e5

QD
type: SiteQuality
SIO_000300: 1.392e1

VQSLOD
type: SiteQuality
SIO_000300: 3.23e-1

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

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

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

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

GenotypeQuality
all individuals: 185
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 363
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 312
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.624671916010499e-4
allele num: 7620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 6.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

QD
type: SiteQuality
SIO_000300: 1.236e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.53e-2

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: 5.29e-1

DP
type: SiteQuality
SIO_000300: 1.79276e5

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

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

GenotypeQuality
all individuals: 342
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 818
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3846
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 9.75e1
variant carriers: 1

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 3.337e1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 9.602e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.49e-2

MQ
type: SiteQuality
SIO_000300: 5.91e1

VQSLOD
type: SiteQuality
SIO_000300: -2.655e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.59e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

DP
type: SiteQuality
SIO_000300: 1.79203e5

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

GenotypeQuality
all individuals: 344
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 203
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 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: 558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.019e0

FS
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.58e-2

QD
type: SiteQuality
SIO_000300: 1.19e1

VQSLOD
type: SiteQuality
SIO_000300: -6.853e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e0

DP
type: SiteQuality
SIO_000300: 1.7923e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 343
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
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: 558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.255e0

DP
type: SiteQuality
SIO_000300: 1.79136e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 5.716e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.285e0

VQSLOD
type: SiteQuality
SIO_000300: 2.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 1.756e1

GenotypeQuality
all individuals: 196
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1528
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3751
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
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: 558
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.937007874015748e-4
allele num: 7620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

FS
type: SiteQuality
SIO_000300: 4.3e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

DP
type: SiteQuality
SIO_000300: 1.78477e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.32e-1

QD
type: SiteQuality
SIO_000300: 1.541e1

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

GenotypeQuality
all individuals: 301
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 201
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3763
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.767017155506364e-4
allele num: 3614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.912e0

VQSLOD
type: SiteQuality
SIO_000300: 7.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-2

FS
type: SiteQuality
SIO_000300: 3.207e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

QD
type: SiteQuality
SIO_000300: 1.154e1

MQ
type: SiteQuality
SIO_000300: 5.987e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.55e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.78e-1

DP
type: SiteQuality
SIO_000300: 1.78502e5

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3762
bin: 6.25e1
variant carriers: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
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: 132
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.78115e5

BaseQRankSum
type: SiteQuality
SIO_000300: -4.992e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

QD
type: SiteQuality
SIO_000300: 1.302e1

MQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.25e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 3.657e0

VQSLOD
type: SiteQuality
SIO_000300: 5.85e-1

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1540
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3753
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312335958005249e-4
allele num: 7620
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: 132
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3616
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.678e0

QD
type: SiteQuality
SIO_000300: 1.214e1

FS
type: SiteQuality
SIO_000300: 6.983e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.64e-1

DP
type: SiteQuality
SIO_000300: 1.77962e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.32e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.3e-2

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-2

GenotypeQuality
all individuals: 201
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3626
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-2

DP
type: SiteQuality
SIO_000300: 1.7847e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.37e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.538e0

VQSLOD
type: SiteQuality
SIO_000300: 3.55e-1

QD
type: SiteQuality
SIO_000300: 1.128e1

FS
type: SiteQuality
SIO_000300: 9.85e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-3

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

GenotypeQuality
all individuals: 1507
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 795
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 183
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 146
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313370107696349e-4
allele num: 7614
num of homozygotes: 0

Latino
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: 3584
num of homozygotes: 0

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

East Asian
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: 2
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.75551e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.43e-2

FS
type: SiteQuality
SIO_000300: 1.141e0

VQSLOD
type: SiteQuality
SIO_000300: -2.947e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.905e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: -1.154e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e0

QD
type: SiteQuality
SIO_000300: 1.197e1

MQ
type: SiteQuality
SIO_000300: 5.875e1

GenotypeQuality
all individuals: 181
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 73
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1578
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 6.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.796420581655481e-4
allele num: 3576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.69e-1

DP
type: SiteQuality
SIO_000300: 1.74711e5

MQ
type: SiteQuality
SIO_000300: 6.025e1

FS
type: SiteQuality
SIO_000300: 5.035e0

QD
type: SiteQuality
SIO_000300: 1.632e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.43e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.733e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.25e-1

GenotypeQuality
all individuals: 764
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 196
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3255
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3548
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.315097317201473e-4
allele num: 7604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

East Asian
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: NaN
allele num: 0
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 3.42e-1

DP
type: SiteQuality
SIO_000300: 1.72139e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.34e-2

FS
type: SiteQuality
SIO_000300: 9.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

MQRankSum
type: SiteQuality
SIO_000300: -3.53e-1

QD
type: SiteQuality
SIO_000300: 1.445e1

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3212
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.630886608787161e-4
allele num: 7602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

East Asian
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: 3546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.42e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.162e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.666e1

DP
type: SiteQuality
SIO_000300: 1.71644e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1954
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3384
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

South Asian
type: Population
allele count: 6
allele frequency: 7.896814951302974e-4
allele num: 7598
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.27e0

FS
type: SiteQuality
SIO_000300: 2.243e0

DP
type: SiteQuality
SIO_000300: 1.73531e5

QD
type: SiteQuality
SIO_000300: 1.359e1

VQSLOD
type: SiteQuality
SIO_000300: 3.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
all individuals: 1883
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3367
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.630630630630631e-4
allele num: 3552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.401e1

VQSLOD
type: SiteQuality
SIO_000300: -9.279999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.08e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.91e-1

DP
type: SiteQuality
SIO_000300: 1.73591e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

FS
type: SiteQuality
SIO_000300: 7.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.87e0

GenotypeQuality
all individuals: 1928
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 305
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 7.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.319148936170213e-3
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3552
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.219e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: 7.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.44e0

DP
type: SiteQuality
SIO_000300: 1.74747e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.03e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.244e0

QD
type: SiteQuality
SIO_000300: 1.441e1

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

GenotypeQuality
all individuals: 363
bin: 9.75e1
variant carriers: 24

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 204
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 198
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

South Asian
type: Population
allele count: 26
allele frequency: 3.42015259142331e-3
allele num: 7602
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.64e-2

QD
type: SiteQuality
SIO_000300: 1.56e1

MQRankSum
type: SiteQuality
SIO_000300: 2.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.727e0

FS
type: SiteQuality
SIO_000300: 1.151e0

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

DP
type: SiteQuality
SIO_000300: 1.753e5

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeQuality
all individuals: 137
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1884
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 811
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.315097317201473e-4
allele num: 7604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.813731007315701e-4
allele num: 3554
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.39e-1

DP
type: SiteQuality
SIO_000300: 1.74898e5

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.88e-2

FS
type: SiteQuality
SIO_000300: 6.443e0

QD
type: SiteQuality
SIO_000300: 1.243e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.348e0

VQSLOD
type: SiteQuality
SIO_000300: 1.76e-1

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1777
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 341
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.813731007315701e-4
allele num: 3554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.88e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

DP
type: SiteQuality
SIO_000300: 1.74191e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

FS
type: SiteQuality
SIO_000300: 7.025e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

QD
type: SiteQuality
SIO_000300: 1.448e1

GenotypeQuality
all individuals: 73
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 204
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3503
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 207
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 1.314060446780552e-4
allele num: 7610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3554
num of homozygotes: 0

African
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: 176
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.74189e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 3.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.105e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.42e-1

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.319148936170213e-3
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3550
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.93e-1

QD
type: SiteQuality
SIO_000300: 1.296e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

DP
type: SiteQuality
SIO_000300: 1.73311e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.61e-2

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 343
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3496
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3572
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313370107696349e-4
allele num: 7614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.85e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.56e0

DP
type: SiteQuality
SIO_000300: 1.7415e5

QD
type: SiteQuality
SIO_000300: 1.519e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.11e-1

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

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 8.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313370107696349e-4
allele num: 7614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3580
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

FS
type: SiteQuality
SIO_000300: 1.441e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.919e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.694e0

DP
type: SiteQuality
SIO_000300: 1.74784e5

MQRankSum
type: SiteQuality
SIO_000300: -8.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.89e-2

MQ
type: SiteQuality
SIO_000300: 5.917e1

QD
type: SiteQuality
SIO_000300: 1.469e1

GenotypeQuality
all individuals: 1801
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 836
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 350
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 184
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3722
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 8.314855875831486e-4
allele num: 3608
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.16e0

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.61e-2

QD
type: SiteQuality
SIO_000300: 1.272e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 1.77792e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 6

GenotypeQuality
all individuals: 236
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 10

GenotypeQuality
all individuals: 147
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1382
bin: 9.75e1
variant carriers: 1164

GenotypeQuality
all individuals: 259
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 668
bin: 6.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 82
bin: 8.75e1
variant carriers: 2

African
type: Population
allele count: 75
allele frequency: 1.353790613718412e-1
allele num: 554
num of homozygotes: 2

Other
type: Population
allele count: 8
allele frequency: 6.060606060606061e-2
allele num: 132
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 4.545454545454546e-2
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 22
allele frequency: 1.182795698924731e-1
allele num: 186
num of homozygotes: 2

South Asian
type: Population
allele count: 691
allele frequency: 9.068241469816272e-2
allele num: 7620
num of homozygotes: 35

European (Non-Finnish)
type: Population
allele count: 430
allele frequency: 1.185879757308329e-1
allele num: 3626
num of homozygotes: 24

European (Finnish)
type: Population
allele count: 1
allele frequency: 5.0e-1
allele num: 2
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

DP
type: SiteQuality
SIO_000300: 2.21772e5

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.799e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.84e-2

QD
type: SiteQuality
SIO_000300: 1.478e1

GenotypeQuality
all individuals: 381
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 199
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1784
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3913
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
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: 2
allele frequency: 5.518763796909492e-4
allele num: 3624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
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: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.63e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

QD
type: SiteQuality
SIO_000300: 1.314e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.14e-1

FS
type: SiteQuality
SIO_000300: 5.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

DP
type: SiteQuality
SIO_000300: 1.80069e5

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

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3921
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 7.5e0
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
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: 556
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: 132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.359e1

FS
type: SiteQuality
SIO_000300: 7.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.22e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 6.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.61e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.263e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.1e-1

DP
type: SiteQuality
SIO_000300: 1.8014e5

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 200
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1832
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 280
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 380
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3932
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
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

African
type: Population
allele count: 1
allele frequency: 1.798561151079137e-3
allele num: 556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.293e0

QD
type: SiteQuality
SIO_000300: 1.936e1

MQ
type: SiteQuality
SIO_000300: 5.502e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.80189e5

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.83e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.39e-1

GenotypeQuality
all individuals: 179
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 67
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 380
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 279
bin: 7.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
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: 2.759381898454746e-4
allele num: 3624
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: 556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.80042e5

FS
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: -1.694e0

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.82e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.72e-1

MQ
type: SiteQuality
SIO_000300: 5.81e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

QD
type: SiteQuality
SIO_000300: 1.25e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.07e-1

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

GenotypeQuality
all individuals: 3932
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 831
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 55
bin: 2.25e1
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: 198
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: 556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 8.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.72e-2

MQ
type: SiteQuality
SIO_000300: 5.988e1

QD
type: SiteQuality
SIO_000300: 1.434e1

MQRankSum
type: SiteQuality
SIO_000300: 1.51e0

VQSLOD
type: SiteQuality
SIO_000300: -2.295e-1

DP
type: SiteQuality
SIO_000300: 1.79818e5

BaseQRankSum
type: SiteQuality
SIO_000300: 5.82e0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3907
bin: 6.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
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: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.892e1

FS
type: SiteQuality
SIO_000300: 2.259e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.73e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.01e-1

QD
type: SiteQuality
SIO_000300: 1.168e1

MQRankSum
type: SiteQuality
SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: -1.598e0

DP
type: SiteQuality
SIO_000300: 1.79095e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e-1

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3904
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.76243093922652e-4
allele num: 3620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
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: 7618
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.792e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.475e0

DP
type: SiteQuality
SIO_000300: 1.78982e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.67e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

QD
type: SiteQuality
SIO_000300: 1.064e1

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
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: 556
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 7.876082961407193e-4
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.11e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 1.2807e1

QD
type: SiteQuality
SIO_000300: 1.406e1

DP
type: SiteQuality
SIO_000300: 1.79016e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.53e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.419e0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 9.75e1
variant carriers: 12

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

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 97
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 12
allele frequency: 1.575216592281439e-3
allele num: 7618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 1.79159e5

QD
type: SiteQuality
SIO_000300: 1.04e1

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

FS
type: SiteQuality
SIO_000300: 5.45e-1

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313370107696349e-4
allele num: 7614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.78034e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.08e-2

FS
type: SiteQuality
SIO_000300: 5.545e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.41e0

MQRankSum
type: SiteQuality
SIO_000300: -2.42e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

QD
type: SiteQuality
SIO_000300: 1.151e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.31e-1

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3844
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1381
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.175e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.33e0

FS
type: SiteQuality
SIO_000300: 1.051e0

DP
type: SiteQuality
SIO_000300: 1.7771e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.09e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.231e1

VQSLOD
type: SiteQuality
SIO_000300: -9.432e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1601
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 809
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.41e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.29e-1

DP
type: SiteQuality
SIO_000300: 1.78006e5

QD
type: SiteQuality
SIO_000300: 1.079e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e-1

FS
type: SiteQuality
SIO_000300: 3.178e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.169e0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1522
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 159
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 1.444043321299639e-2
allele num: 554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
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: 3620
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.090000000000001e-1

FS
type: SiteQuality
SIO_000300: 2.515e0

DP
type: SiteQuality
SIO_000300: 1.78559e5

VQSLOD
type: SiteQuality
SIO_000300: 7.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.04e-2

QD
type: SiteQuality
SIO_000300: 1.304e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.834e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3855
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1558
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 279
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313025210084034e-4
allele num: 7616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
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: 2
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.55e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 1.739e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 7.93e-1

DP
type: SiteQuality
SIO_000300: 1.7832e5

VQSLOD
type: SiteQuality
SIO_000300: 2.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.52e-2

GenotypeQuality
all individuals: 1192
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3896
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.805054151624549e-3
allele num: 554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: -5.663e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.83e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 7.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.49e-1

FS
type: SiteQuality
SIO_000300: 6.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.305e0

DP
type: SiteQuality
SIO_000300: 1.7765e5

GenotypeQuality
all individuals: 330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3899
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Latino
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: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.524861878453039e-4
allele num: 3620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7616
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.85e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e0

DP
type: SiteQuality
SIO_000300: 1.77613e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.26e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.25e-2

QD
type: SiteQuality
SIO_000300: 8.83e0

GenotypeQuality
all individuals: 1214
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 279
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 2.626050420168067e-4
allele num: 7616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.105583195135434e-3
allele num: 3618
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.340000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.698e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 1.7793e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.77e-2

MQRankSum
type: SiteQuality
SIO_000300: -6.75e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.15e1

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeQuality
all individuals: 162
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3642
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.313715186547556e-4
allele num: 7612
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.105e1

VQSLOD
type: SiteQuality
SIO_000300: 2.29e-1

FS
type: SiteQuality
SIO_000300: 6.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.09e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.834e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.12e-1

DP
type: SiteQuality
SIO_000300: 1.76198e5

GenotypeQuality
all individuals: 210
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 572
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 95
bin: 2.25e1
variant carriers: 8

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 7

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 115
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1337
bin: 7.5e0
variant carriers: 27

GenotypeQuality
all individuals: 63
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 198
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1856
bin: 9.75e1
variant carriers: 1802

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 13
allele frequency: 9.848484848484848e-2
allele num: 132
num of homozygotes: 0

East Asian
type: Population
allele count: 56
allele frequency: 2.828282828282828e-1
allele num: 198
num of homozygotes: 12

European (Non-Finnish)
type: Population
allele count: 421
allele frequency: 1.168146503884573e-1
allele num: 3604
num of homozygotes: 24

Latino
type: Population
allele count: 30
allele frequency: 1.630434782608696e-1
allele num: 184
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
type: Population
allele count: 28
allele frequency: 5.109489051094891e-2
allele num: 548
num of homozygotes: 1

South Asian
type: Population
allele count: 1462
allele frequency: 1.920147097452062e-1
allele num: 7614
num of homozygotes: 151

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.42e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.56e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

QD
type: SiteQuality
SIO_000300: 1.688e1

DP
type: SiteQuality
SIO_000300: 2.32656e5

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1569
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 912
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 9.75e1
variant carriers: 9

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

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

South Asian
type: Population
allele count: 9
allele frequency: 1.18172268907563e-3
allele num: 7616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

DP
type: SiteQuality
SIO_000300: 1.7466e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.53e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.25e-1

QD
type: SiteQuality
SIO_000300: 1.593e1

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: 2.6e0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3950
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 9.75e1
variant carriers: 10

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 2.768549280177187e-3
allele num: 3612
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.409e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.57e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

QD
type: SiteQuality
SIO_000300: 1.174e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.48e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 5.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.49e-1

DP
type: SiteQuality
SIO_000300: 1.74719e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

GenotypeQuality
all individuals: 181
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 921
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1611
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3980
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313025210084034e-4
allele num: 7616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.893e0

QD
type: SiteQuality
SIO_000300: 8.69e0

DP
type: SiteQuality
SIO_000300: 1.74586e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

MQ
type: SiteQuality
SIO_000300: 5.848e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.63e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

GenotypeQuality
all individuals: 3992
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 146
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 9.75e1
variant carriers: 37

GenotypeQuality
all individuals: 78
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 4.545454545454546e-2
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 28
allele frequency: 3.676470588235294e-3
allele num: 7616
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.765486725663717e-4
allele num: 3616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.59e0

FS
type: SiteQuality
SIO_000300: 5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.5e0

DP
type: SiteQuality
SIO_000300: 1.7593e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.19e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

QD
type: SiteQuality
SIO_000300: 1.194e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 76
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.382743362831858e-3
allele num: 3616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.985e1

FS
type: SiteQuality
SIO_000300: 1.103e0

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.52e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 1.74245e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: 7.24e-1

QD
type: SiteQuality
SIO_000300: 1.299e1

GenotypeQuality
all individuals: 78
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1585
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 77
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.544e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.188e0

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.903e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.225e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.57e-2

DP
type: SiteQuality
SIO_000300: 1.74143e5

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

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4017
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 74
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 141
bin: 9.75e1
variant carriers: 39

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

South Asian
type: Population
allele count: 38
allele frequency: 4.988185875557889e-3
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.74233e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

FS
type: SiteQuality
SIO_000300: 1.162e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.48e-2

QD
type: SiteQuality
SIO_000300: 1.563e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 933
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.72e-2

FS
type: SiteQuality
SIO_000300: 2.504e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.52e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 1.73066e5

QD
type: SiteQuality
SIO_000300: 1.272e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.953e0

GenotypeQuality
all individuals: 102
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1625
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4013
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.313025210084034e-4
allele num: 7616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3616
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.791e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.56e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.344e0

MQRankSum
type: SiteQuality
SIO_000300: -4.15e-1

DP
type: SiteQuality
SIO_000300: 1.7296e5

FS
type: SiteQuality
SIO_000300: 4.638e0

QD
type: SiteQuality
SIO_000300: 2.247e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e0

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

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

GenotypeQuality
all individuals: 1571
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 142
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 1.72579e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.25e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

QD
type: SiteQuality
SIO_000300: 8.220000000000001e0

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

GenotypeQuality
all individuals: 299
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4061
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.211e0

VQSLOD
type: SiteQuality
SIO_000300: -4.958e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.448e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.46e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.71719e5

QD
type: SiteQuality
SIO_000300: 1.558e1