19-36504174-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504174
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504174
    reference: chr 19
allele count: 7
allele frequency: 5.916659623024258e-5
allele num: 118310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+72C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+72C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.113+38C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+72C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.176C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+72C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-183C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+72C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.189C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+72C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+72C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+72C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000462793
  gene symbol: ALKBH6
  hgvsc: ENST00000462793.1:n.32C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+72C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+72C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+56C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+72C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-183C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+72C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+72C>T
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

19-36504175-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504175
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504175
    reference: chr 19
allele count: 4282
allele frequency: 3.620468073593074e-2
allele num: 118272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+71C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+71C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+71C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+71C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.175C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+71C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+71C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.188C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+71C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000462793
  gene symbol: ALKBH6
  hgvsc: ENST00000462793.1:n.31C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.113+37C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+71C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+71C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-184C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+71C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+71C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+55C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-184C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+71C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+71C>T
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 270
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

19-36504177-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504177
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504177
    reference: chr 19
allele count: 2
allele frequency: 1.68947457340767e-5
allele num: 118380
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+69C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+69C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+69C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000462793
  gene symbol: ALKBH6
  hgvsc: ENST00000462793.1:n.29C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+69C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+69C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+69C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+69C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+69C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.186C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+69C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+53C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.113+35C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-186C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+69C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+69C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.173C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+69C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+69C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-186C>G
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-36504195-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504195
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504195
    reference: chr 19
allele count: 11
allele frequency: 9.182429837888376e-5
allele num: 119794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+35G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+51G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+51G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+51G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+51G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+51G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-204G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+51G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.168G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000462793
  gene symbol: ALKBH6
  hgvsc: ENST00000462793.1:n.11G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+51G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+51G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-204G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+51G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.155G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+51G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+51G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+51G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.113+17G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+51G>T
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

19-36504196-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504196
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504196
    reference: chr 19
allele count: 2
allele frequency: 1.667639456349537e-5
allele num: 119930
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+34A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-205A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+50A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+50A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+50A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.113+16A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.154A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+50A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+50A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-205A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+50A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.167A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000462793
  gene symbol: ALKBH6
  hgvsc: ENST00000462793.1:n.10A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+50A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+50A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+50A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+50A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+50A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+50A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+50A>G
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
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: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-36504198-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504198
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504198
    reference: chr 19
allele count: 5
allele frequency: 4.163197335553705e-5
allele num: 120100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-207T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.152T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+48T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000462793
  gene symbol: ALKBH6
  hgvsc: ENST00000462793.1:n.8T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+48T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.165T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+32T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+48T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+48T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+48T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.113+14T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+48T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+48T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+48T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-207T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+48T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+48T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+48T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+48T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+48T>C
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

19-36504208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504208
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504208
    reference: chr 19
allele count: 15
allele frequency: 1.243203819122132e-4
allele num: 120656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+38G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+38G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-217G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.113+4G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+38G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+38G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+38G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+38G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.142G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+38G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.155G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-217G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+38G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+38G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+38G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+38G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+38G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+38G>A
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10657
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.113+4G>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ

19-36504216-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504216
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504216
    reference: chr 19
allele count: 1
allele frequency: 8.265692417053776e-6
allele num: 120982
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.109A>C
  hgvsp: ENSP00000433885.1:p.Glu37Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+30A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+30A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-225A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+30A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+30A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+30A>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-225A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.134A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+30A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+30A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.147A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+30A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+30A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+30A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+30A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+14A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+30A>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+30A>C
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20094
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu37Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-36504219-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504219
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504220
    reference: chr 19
allele count: 2
allele frequency: 1.65264671371201e-5
allele num: 121018
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+26dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+26dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+26dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+26dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.143dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-229dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+26dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.130dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+26dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+26dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+26dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.105dupG
  hgvsp: ENSP00000433885.1:p.Glu37Ter
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-229dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+26dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+10dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+26dupG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+26dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+26dupG
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+26dupG
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu37Ter
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

19-36504222-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504222
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504222
    reference: chr 19
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+24G>C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+8G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.103G>C
  hgvsp: ENSP00000433885.1:p.Glu35Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+24G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+24G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+24G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+24G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-231G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+24G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+24G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.128G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+24G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.141G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+24G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+24G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+24G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+24G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+24G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-231G>C
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu35Asp
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP

19-36504227-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504227
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504227
    reference: chr 19
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-236G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+3G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.98G>A
  hgvsp: ENSP00000433885.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+19G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.136G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.123G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-236G>A
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala34Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

19-36504229-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504229
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504229
    reference: chr 19
allele count: 3
allele frequency: 2.476269087907552e-5
allele num: 121150
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+17G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.121G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+17G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+17G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-238G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+17G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.134G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+17G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+17G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+17G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+17G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+17G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+1G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+17G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+17G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+17G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+17G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-238G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.96G>C
  hgvsp: ENSP00000433885.1:p.Gly33Ala
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16158
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.123+1G>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

19-36504229-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504229
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504229
    reference: chr 19
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.96G>A
  hgvsp: ENSP00000433885.1:p.Gly33Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.138+17G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.140+17G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.54+17G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.113+17G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.123+17G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.121G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-238G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.123+1G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.140+17G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.154+17G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-238G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.134G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.118+17G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.54+17G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.95+17G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.118+17G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.118+17G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.54+17G>A
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.123+1G>A
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/19-36504256-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504256
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504256
    reference: chr 19
allele count: 9
allele frequency: 7.4223131226496e-5
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-265G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.44G>T
  hgvsp: ENSP00000436742.1:p.Arg15Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.108G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.108G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.103G>T
  hgvsp: ENSP00000435496.1:p.Arg35Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.144G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.130G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.94G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.108G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.128G>T
  hgvsp: ENSP00000368152.3:p.Arg43Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.44G>T
  hgvsp: ENSP00000474158.1:p.Arg15Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.69G>T
  hgvsp: ENSP00000433885.1:p.Arg24Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.85G>T
  hgvsp: ENSP00000436156.1:p.Arg29Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-265G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.113G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.97G>T
  hgvsp: ENSP00000433085.1:p.Arg33Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.130G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.44G>T
  hgvsp: ENSP00000252984.6:p.Arg15Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.107G>T
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg43Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

19-36504258-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504258
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504258
    reference: chr 19
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.67C>G
  hgvsp: ENSP00000433885.1:p.Phe23Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.95C>G
  hgvsp: ENSP00000433085.1:p.Phe32Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.128C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.128C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.83C>G
  hgvsp: ENSP00000436156.1:p.Phe28Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.105C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.42C>G
  hgvsp: ENSP00000252984.6:p.Phe14Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.142C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.92C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-267C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.126C>G
  hgvsp: ENSP00000368152.3:p.Phe42Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.106C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.111C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-267C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.42C>G
  hgvsp: ENSP00000436742.1:p.Phe14Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.42C>G
  hgvsp: ENSP00000474158.1:p.Phe14Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.101C>G
  hgvsp: ENSP00000435496.1:p.Phe34Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.106C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.106C>G
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Phe42Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

19-36504261-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504261
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504261
    reference: chr 19
allele count: 3
allele frequency: 2.474226804123711e-5
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.125G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.125G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.80G>A
  hgvsp: ENST00000497999.1:c.80G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.89G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.64G>A
  hgvsp: ENST00000461668.1:c.64G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.123G>A
  hgvsp: ENST00000378875.3:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.92G>A
  hgvsp: ENST00000481257.1:c.92G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.39G>A
  hgvsp: ENST00000486389.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.98G>A
  hgvsp: ENST00000490986.1:c.98G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.39G>A
  hgvsp: ENST00000252984.7:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.39G>A
  hgvsp: ENST00000485128.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.103G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.102G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-270G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.103G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.139G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.103G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.108G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-270G>A
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro41Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

19-36504262-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504262
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504262
    reference: chr 19
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.38C>T
  hgvsp: ENSP00000474158.1:p.Pro13Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.38C>T
  hgvsp: ENSP00000436742.1:p.Pro13Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.79C>T
  hgvsp: ENSP00000436156.1:p.Pro27Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-271C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.97C>T
  hgvsp: ENSP00000435496.1:p.Pro33Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.107C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.124C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.102C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.88C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.63C>T
  hgvsp: ENSP00000433885.1:p.Pro22Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.38C>T
  hgvsp: ENSP00000252984.6:p.Pro13Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.122C>T
  hgvsp: ENSP00000368152.3:p.Pro41Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.138C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.124C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-271C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.101C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.102C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.91C>T
  hgvsp: ENSP00000433085.1:p.Pro31Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.102C>T
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro41Leu
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

19-36504271-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504271
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504271
    reference: chr 19
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.93C>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.113C>A
  hgvsp: ENSP00000368152.3:p.Ala38Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.79C>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.29C>A
  hgvsp: ENSP00000474158.1:p.Ala10Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-280C>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.115C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.93C>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.54C>A
  hgvsp: ENSP00000433885.1:p.Ala19Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.115C>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.88C>A
  hgvsp: ENSP00000435496.1:p.Ala30Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.29C>A
  hgvsp: ENSP00000252984.6:p.Ala10Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.29C>A
  hgvsp: ENSP00000436742.1:p.Ala10Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.70C>A
  hgvsp: ENSP00000436156.1:p.Ala24Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.93C>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.92C>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.98C>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-280C>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.129C>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.82C>A
  hgvsp: ENSP00000433085.1:p.Ala28Asp
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala38Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

19-36504284-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504284
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504284
    reference: chr 19
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.69G>A
  hgvsp: ENSP00000433085.1:p.Ala24Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.16G>A
  hgvsp: ENSP00000474158.1:p.Ala6Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-293G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.116G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.100G>A
  hgvsp: ENSP00000368152.3:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-293G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.57G>A
  hgvsp: ENSP00000436156.1:p.Ala20Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.66G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.102G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.41G>A
  hgvsp: ENSP00000433885.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.80G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.80G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.80G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.79G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.85G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.75G>A
  hgvsp: ENSP00000435496.1:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.16G>A
  hgvsp: ENSP00000436742.1:p.Ala6Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.102G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.16G>A
  hgvsp: ENSP00000252984.6:p.Ala6Thr
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala34Thr
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

19-36504285-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504285
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504285
    reference: chr 19
allele count: 3
allele frequency: 2.475656048852946e-5
allele num: 121180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.65C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.79C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-294C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.99C>T
  hgvsp: ENST00000378875.3:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.15C>T
  hgvsp: ENST00000486389.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.78C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.101C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.74C>T
  hgvsp: ENST00000490986.1:c.74C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.101C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.84C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.40C>T
  hgvsp: ENST00000461668.1:c.40C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.15C>T
  hgvsp: ENST00000485128.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.79C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-294C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.79C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.115C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.68C>T
  hgvsp: ENST00000481257.1:c.68C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.56C>T
  hgvsp: ENST00000497999.1:c.56C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.15C>T
  hgvsp: ENST00000252984.7:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp33Asp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-36504290-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504290
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504290
    reference: chr 19
allele count: 3
allele frequency: 2.476309967973058e-5
allele num: 121148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.51C>G
  hgvsp: ENSP00000436156.1:p.Gln18Glu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.96C>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-299C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.94C>G
  hgvsp: ENSP00000368152.3:p.Gln32Glu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.96C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.110C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.79C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-299C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.63C>G
  hgvsp: ENSP00000433085.1:p.Gln22Glu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.35C>G
  hgvsp: ENSP00000433885.1:p.Gln13Glu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.69C>G
  hgvsp: ENSP00000435496.1:p.Gln24Glu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.74C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.74C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.10C>G
  hgvsp: ENSP00000474158.1:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.10C>G
  hgvsp: ENSP00000252984.6:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.10C>G
  hgvsp: ENSP00000436742.1:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.73C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.60C>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.74C>G
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gln32Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

19-36504297-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504297
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504297
    reference: chr 19
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.62G>A
  hgvsp: ENSP00000435496.1:p.Met21Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.53G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.3G>A
  hgvsp: ENSP00000474158.1:p.Met1?
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.72G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.89G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.67G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.56G>A
  hgvsp: ENSP00000433085.1:p.Met19Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-306G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.3G>A
  hgvsp: ENSP00000252984.6:p.Met1?
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.28G>A
  hgvsp: ENSP00000433885.1:p.Met10Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.87G>A
  hgvsp: ENSP00000368152.3:p.Met29Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.66G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.3G>A
  hgvsp: ENSP00000436742.1:p.Met1?
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.67G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.44G>A
  hgvsp: ENSP00000436156.1:p.Met15Ile
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-306G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.89G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.103G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.67G>A
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/19-36504305-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504305
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504305
    reference: chr 19
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.95G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-6G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.81G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.20G>T
  hgvsp: ENSP00000433885.1:p.Val8Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.58G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.36G>T
  hgvsp: ENSP00000436156.1:p.Val13Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.48G>T
  hgvsp: ENSP00000433085.1:p.Val17Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.64G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-6G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-6G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.45G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.59G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.79G>T
  hgvsp: ENSP00000368152.3:p.Val27Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.54G>T
  hgvsp: ENSP00000435496.1:p.Val19Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.81G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-314G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.59G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-314G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.59G>T
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val27Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

19-36504322-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504322
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504322
    reference: chr 19
allele count: 1
allele frequency: 8.274036074797286e-6
allele num: 120860
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.37T>C
  hgvsp: ENSP00000435496.1:p.Ile13Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-23T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-23T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.47T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-331T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-23T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.64T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.62T>C
  hgvsp: ENSP00000368152.3:p.Ile21Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.28T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.31T>C
  hgvsp: ENSP00000433085.1:p.Ile11Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-331T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.19T>C
  hgvsp: ENSP00000436156.1:p.Ile7Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433885
  ensembl transcript: ENST00000461668
  gene symbol: ALKBH6
  hgvsc: ENST00000461668.1:c.3T>C
  hgvsp: ENSP00000433885.1:p.Ile2Thr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.42T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.78T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.42T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.42T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.41T>C
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile21Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

19-36504329-AGGGAGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504329
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504323
    reference: chr 19
allele count: 3
allele frequency: 2.486572508454347e-5
allele num: 120648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.40-11_40-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.40-11_40-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-25-11_-25-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-25-11_-25-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.76-11_76-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.35-11_35-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.62-11_62-6delCCTCCC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.40-11_40-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-344_10-339delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.29-11_29-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.26-11_26-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.62-11_62-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.39-11_39-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-344_49-339delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.17-11_17-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-25-11_-25-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.60-11_60-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.45-11_45-6delCCTCCC
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.60-11_60-6delCCTCCC
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: AGGGAGG
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

19-36504342-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504342
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504342
    reference: chr 19
allele count: 1
allele frequency: 8.304820117596252e-6
allele num: 120412
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.60-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.39-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.76-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.45-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.40-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-351G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.62-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.17-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.40-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-25-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.29-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-351G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.35-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.26-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-25-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.62-18G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.40-18G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-25-18G>C
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

19-36504346-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504346
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504346
    reference: chr 19
allele count: 1
allele frequency: 8.312966565248474e-6
allele num: 120294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-355G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.62-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.29-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.40-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.40-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-355G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-25-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.76-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-25-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-25-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.60-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.17-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.62-22G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.39-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.35-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.26-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.40-22G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.45-22G>A
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

19-36504347-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504347
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504347
    reference: chr 19
allele count: 4
allele frequency: 3.324026060364313e-5
allele num: 120336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.76-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.40-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-25-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.39-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.35-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-356A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-25-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-356A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.62-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.45-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.40-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.26-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.62-23A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-25-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.60-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.29-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.40-23A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.17-23A>G
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-36504355-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504355
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504355
    reference: chr 19
allele count: 1
allele frequency: 8.324731111185109e-6
allele num: 120124
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-25-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.62-31G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-25-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.35-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-25-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.60-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.40-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-364G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.29-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.76-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.17-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.40-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-364G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.39-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.62-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.26-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.45-31G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.40-31G>C
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/19-36504365-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504365
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504365
    reference: chr 19
allele count: 2
allele frequency: 1.670397220459025e-5
allele num: 119732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.62-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.35-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-25-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.40-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-374G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.45-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.62-41G>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.60-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.26-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.17-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-25-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.40-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-374G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-25-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.76-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.40-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.29-41G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.39-41G>T
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

19-36504365-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504365
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504365
    reference: chr 19
allele count: 567
allele frequency: 4.735576120001336e-3
allele num: 119732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.45-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.40-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-374G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.60-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.26-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-374G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.62-41G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.39-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-25-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-25-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.17-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.35-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.62-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.40-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.40-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-25-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.76-41G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.29-41G>A
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14345
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 4.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 14
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

19-36504366-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504366
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504366
    reference: chr 19
allele count: 45
allele frequency: 3.759838243403573e-4
allele num: 119686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.40-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-375C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.40-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.40-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.76-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.45-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-25-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.35-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-375C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.62-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.62-42C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.60-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.39-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-25-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.29-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.17-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.26-42C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-25-42C>T
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 3.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

19-36504373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36504373
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36504373
    reference: chr 19
allele count: 2
allele frequency: 1.674284661878213e-5
allele num: 119454
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.40-49G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-26+43G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.45-49G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.35-49G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.62-49G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.17-49G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.39-49G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.26-49G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.49-382G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.40-49G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000468004
  gene symbol: ALKBH6
  hgvsc: ENST00000468004.1:n.75+43G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-26+43G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.62-49G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-26+43G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.60-49G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.40-49G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.29-49G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.10-382G>A
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

19-36505035-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505035
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505036
    reference: chr 19
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: TG
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.61+41_61+42insC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.61+41_61+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.48+41_48+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.44+41_44+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.39+41_39+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.38+41_38+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-646_-645insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-101+41_-101+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.25+41_25+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.59+41_59+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-101+41_-101+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.16+41_16+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.39+41_39+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.28+41_28+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.34+41_34+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.9+41_9+42insC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.39+41_39+42insC
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

19-36505036-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505036
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505036
    reference: chr 19
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.61+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-101+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.44+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.39+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.59+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.16+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.34+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-646T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.28+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.25+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.48+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.39+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.38+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.61+41T>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.9+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.39+41T>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-101+41T>A
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

19-36505050-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505050
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505050
    reference: chr 19
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.28+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.44+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-660G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.38+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.61+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.34+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.25+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-101+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.48+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-101+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.39+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.9+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.39+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.39+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.16+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.59+27G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.61+27G>C
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS

19-36505051-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505051
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505051
    reference: chr 19
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.48+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.39+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.38+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.9+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.39+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-661A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.39+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.59+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.44+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.16+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.25+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-101+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.28+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.34+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.61+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-101+26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.61+26A>G
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/19-36505053-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505053
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505053
    reference: chr 19
allele count: 7
allele frequency: 5.76948437293947e-5
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.39+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.61+24G>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.59+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-663G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.44+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.34+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.16+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.61+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.28+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.48+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.39+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.9+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.39+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.25+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-101+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-101+24G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.38+24G>T
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

19-36505055-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505055
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505055
    reference: chr 19
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-101+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.9+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-665G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.39+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.59+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.16+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.38+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.61+22G>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.34+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.39+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.61+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-101+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.39+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.28+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.25+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.44+22G>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.48+22G>C
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

19-36505058-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505058
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505057
    reference: chr 19
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.38+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.39+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.39+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.28+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.34+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.59+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.39+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.61+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-669delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.25+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.44+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.9+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.48+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-101+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.16+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-101+18delC
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.61+18delC
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14843
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: AG
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-36505077-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505077
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505077
    reference: chr 19
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-101G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.34G>T
  hgvsp: ENSP00000435496.1:p.Arg12Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.44G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.38G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.61G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.61G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.28G>T
  hgvsp: ENSP00000433085.1:p.Arg10Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.48G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-101G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.16G>T
  hgvsp: ENSP00000436156.1:p.Arg6Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.25G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.59G>T
  hgvsp: ENSP00000368152.3:p.Arg20Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.39G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-687G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.9G>T
  hgvsp: ENST00000490483.1:c.9G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.39G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.39G>T
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg20Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

19-36505083-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505083
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505083
    reference: chr 19
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.53G>A
  hgvsp: ENSP00000368152.3:p.Gly18Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.28G>A
  hgvsp: ENSP00000435496.1:p.Gly10Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-107G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.55G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.22G>A
  hgvsp: ENSP00000433085.1:p.Gly8Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.42G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433156
  ensembl transcript: ENST00000490483
  gene symbol: ALKBH6
  hgvsc: ENST00000490483.1:c.3G>A
  hgvsp: ENSP00000433156.1:p.Trp1?
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.33G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.10G>A
  hgvsp: ENSP00000436156.1:p.Gly4Asp
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-107G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.32G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.33G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.55G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.33G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-693G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.38G>A
  variant of: http://identifiers.org/hgnc/28243
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6470
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp1?
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

19-36505089-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505089
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505089
    reference: chr 19
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.47A>G
  hgvsp: ENSP00000368152.3:p.Asp16Gly
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.16A>G
  hgvsp: ENSP00000433085.1:p.Asp6Gly
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-113A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.32A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.4A>G
  hgvsp: ENSP00000436156.1:p.Asp2Gly
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.13A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.27A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.27A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-699A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.22A>G
  hgvsp: ENSP00000435496.1:p.Asp8Gly
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.49A>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-113A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.36A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.27A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.26A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.49A>G
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6473
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp16Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/19-36505090-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505090
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505090
    reference: chr 19
allele count: 4
allele frequency: 3.295435821387378e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-700G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.3G>T
  hgvsp: ENSP00000436156.1:p.Asp2Tyr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.46G>T
  hgvsp: ENSP00000368152.3:p.Asp16Tyr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.21G>T
  hgvsp: ENSP00000435496.1:p.Asp8Tyr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.26G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-114G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.26G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.25G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.12G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.31G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.26G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-114G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.48G>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.48G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.15G>T
  hgvsp: ENSP00000433085.1:p.Asp6Tyr
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.35G>T
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13816
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp16Tyr
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum

19-36505090-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505090
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505090
    reference: chr 19
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.12G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.21G>A
  hgvsp: ENSP00000435496.1:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-114G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.26G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-700G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.48G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.35G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.31G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.48G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436156
  ensembl transcript: ENST00000497999
  gene symbol: ALKBH6
  hgvsc: ENST00000497999.1:c.3G>A
  hgvsp: ENSP00000436156.1:p.Asp2Asn
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.46G>A
  hgvsp: ENSP00000368152.3:p.Asp16Asn
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.15G>A
  hgvsp: ENSP00000433085.1:p.Asp6Asn
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.26G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.26G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-114G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.25G>A
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp16Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-36505096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505096
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505096
    reference: chr 19
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.9G>A
  hgvsp: ENSP00000433085.1:p.Gly4Arg
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.20G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-120G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.29G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-706G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-120G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.6G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.20G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.15G>A
  hgvsp: ENSP00000435496.1:p.Gly6Arg
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.42G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.40G>A
  hgvsp: ENSP00000368152.3:p.Gly14Arg
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.42G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.25G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.19G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.20G>A
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly14Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

19-36505097-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505097
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505097
    reference: chr 19
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.19T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.41T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.39T>C
  hgvsp: ENST00000378875.3:c.39T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-707T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000592353
  gene symbol: ALKBH6
  hgvsc: ENST00000592353.1:n.5T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.18T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.19T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.19T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-121T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.28T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000435496
  ensembl transcript: ENST00000490986
  gene symbol: ALKBH6
  hgvsc: ENST00000490986.1:c.14T>C
  hgvsp: ENST00000490986.1:c.14T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000433085
  ensembl transcript: ENST00000481257
  gene symbol: ALKBH6
  hgvsc: ENST00000481257.1:c.8T>C
  hgvsp: ENST00000481257.1:c.8T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-121T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.41T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.24T>C
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile13Ile
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

19-36505114-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505114
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505114
    reference: chr 19
allele count: 2
allele frequency: 1.650246711883427e-5
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.11A>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.2A>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-724A>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.22A>T
  hgvsp: ENSP00000368152.3:p.Met8Leu
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.24A>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-138A>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.2A>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.7A>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-138A>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.24A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.1A>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.2A>T
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met8Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum

19-36505114-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505114
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505114
    reference: chr 19
allele count: 69
allele frequency: 5.693351155997822e-4
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000466196
  gene symbol: ALKBH6
  hgvsc: ENST00000466196.1:n.2A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.11A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.22A>G
  hgvsp: ENSP00000368152.3:p.Met8Val
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-138A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000590666
  gene symbol: ALKBH6
  hgvsc: ENST00000590666.1:n.2A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000392183
  gene symbol: ALKBH6
  hgvsc: ENST00000392183.3:n.2A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000471323
  gene symbol: ALKBH6
  hgvsc: ENST00000471323.1:n.1A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.24A>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-724A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-138A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.24A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.7A>G
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6442
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 9.75e1
  variant carriers: 40
genotype quality: GenotypeQuality
hgvs: p.Met8Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

19-36505120-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505120
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505120
    reference: chr 19
allele count: 186
allele frequency: 1.547833033752746e-3
allele num: 120168
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.16A>G
  hgvsp: ENSP00000368152.3:p.Met6Val
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-730A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-144A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-144A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.18A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000470859
  gene symbol: ALKBH6
  hgvsc: ENST00000470859.1:n.1A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.5A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.18A>G
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 13805
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14685
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 9.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6378
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 2.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 13735
  bin: 9.75e1
  variant carriers: 121
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 5.25e1
  variant carriers: 4
hgvs: p.Met6Val
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

19-36505121-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505121
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505121
    reference: chr 19
allele count: 1
allele frequency: 8.247558722618106e-6
allele num: 121248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000495116
  gene symbol: ALKBH6
  hgvsc: ENST00000495116.2:n.4G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.17G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-145G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.15G>A
  hgvsp: ENST00000378875.3:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.17G>A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-145G>A
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-731G>A
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14419
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8489
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3741
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4214
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly5Gly
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

19-36505125-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505125
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505124
    reference: chr 19
allele count: 2
allele frequency: 1.649647800194658e-5
allele num: 121238
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.12delA
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-150delA
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.12delA
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.10delA
  hgvsp: ENSP00000368152.3:p.Arg4GlyfsTer6
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-736delA
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-150delA
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9486
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14412
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3068
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4198
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg4GlyfsTer6
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: CT
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

19-36505126-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505126
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505126
    reference: chr 19
allele count: 572
allele frequency: 5.04569351822448e-3
allele num: 113364
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.12A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.12A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.10A>G
  hgvsp: ENSP00000368152.3:p.Arg4Gly
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000252984
  ensembl transcript: ENST00000252984
  gene symbol: ALKBH6
  hgvsc: ENST00000252984.7:c.-150A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-150A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-736A>G
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 14243
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 9.75e1
  variant carriers: 283
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 6.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 5.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 4.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 9477
  bin: 3.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 4.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 14650
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 3.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 4.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 1887
  bin: 8.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 3709
  bin: 8.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 7814
  bin: 6.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 4471
  bin: 7.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 5.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 7.5e0
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 2660
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 3125
  bin: 2.5e0
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 3375
  bin: 7.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 2.75e1
  variant carriers: 24
hgvs: p.Arg4Gly
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP

19-36505131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505131
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505131
    reference: chr 19
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.7C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.5C>T
  hgvsp: ENSP00000368152.3:p.Ala2Val
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-155C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-741C>T
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.7C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5976
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15568
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8992
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4962
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21501
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3961
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala2Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

19-36505134-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505134
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505134
    reference: chr 19
allele count: 2
allele frequency: 1.651227687785869e-5
allele num: 121122
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.2T>C
  hgvsp: ENSP00000368152.3:p.Met1?
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-744T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.4T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-158T>C
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.4T>C
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9596
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2842
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3962
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1996
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11609
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4956
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

19-36505135-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505135
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505135
    reference: chr 19
allele count: 1
allele frequency: 8.258456659619451e-6
allele num: 121088
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000436742
  ensembl transcript: ENST00000485128
  gene symbol: ALKBH6
  hgvsc: ENST00000485128.1:c.-159A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248101
  ensembl transcript: ENST00000473572
  gene symbol: AC002116.8
  hgvsc: ENST00000473572.2:n.3A>G
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000368152
  ensembl transcript: ENST00000378875
  gene symbol: ALKBH6
  hgvsc: ENST00000378875.3:c.1A>G
  hgvsp: ENSP00000368152.3:p.Met1?
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000239382
  ensembl transcript: ENST00000475223
  gene symbol: ALKBH6
  hgvsc: ENST00000475223.1:n.3A>G
  variant of: http://identifiers.org/hgnc/28243
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000239382
  ensembl protein: ENSP00000474158
  ensembl transcript: ENST00000486389
  gene symbol: ALKBH6
  hgvsc: ENST00000486389.1:c.-745A>G
  variant of: http://identifiers.org/hgnc/28243
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15452
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3961
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4956
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8970
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3721
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2845
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

19-36505143-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505143
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505143
    reference: chr 19
allele count: 1
allele frequency: 8.267605866693123e-6
allele num: 120954
alternate allele: T
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3895
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2819
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1968
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8796
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3655
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11549
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4868
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20944
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10316
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11554
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6608
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 904
  num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

19-36505144-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505144
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505144
    reference: chr 19
allele count: 1
allele frequency: 8.268699664290793e-6
allele num: 120938
alternate allele: T
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11546
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2816
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20738
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4851
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3640
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8758
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3891
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1962
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11552
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 66448
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10314
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8628
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

19-36505149-TACAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505149
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505145
    reference: chr 19
allele count: 1
allele frequency: 8.279242283746192e-6
allele num: 120784
alternate allele: T
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14687
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1943
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19485
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8540
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3864
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4807
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1762
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2806
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11519
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 6.068697657482704e-5
  allele num: 16478
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8628
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 904
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 66352
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
reference allele: TACAG
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

19-36505150-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505150
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505150
    reference: chr 19
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: G
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9252
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3863
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18814
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4806
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11523
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2801
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3568
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8390
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1942
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 8.668515950069348e-5
  allele num: 11536
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8626
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10272
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16478
  num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS

19-36505152-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505152
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505152
    reference: chr 19
allele count: 9
allele frequency: 7.455391905101144e-5
allele num: 120718
alternate allele: G
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13823
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14261
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3557
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4790
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2091
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3856
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11523
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2797
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1940
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18590
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8355
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8620
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 66322
  num of homozygotes: 0
population: African
  type: Population
  allele count: 8
  allele frequency: 7.78816199376947e-4
  allele num: 10272
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16474
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/19-36505154-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505154
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505154
    reference: chr 19
allele count: 8
allele frequency: 6.634709482658528e-5
allele num: 120578
alternate allele: C
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13919
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13354
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9074
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2300
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11521
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3849
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4775
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8243
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3513
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8614
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11530
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10248
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6580
  num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

19-36505154-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505154
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505154
    reference: chr 19
allele count: 2
allele frequency: 1.658677370664632e-5
allele num: 120578
alternate allele: G
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13354
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2300
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11521
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3849
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3513
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8243
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4775
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 2
  allele frequency: 1.95160031225605e-4
  allele num: 10248
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11530
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 66240
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6580
  num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

19-36505154-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505154
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505154
    reference: chr 19
allele count: 15
allele frequency: 1.244008027998474e-4
allele num: 120578
alternate allele: T
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9074
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13354
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2300
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3513
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11521
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 17524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8243
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3849
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4775
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 15
  allele frequency: 2.264492753623188e-4
  allele num: 66240
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8614
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6580
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11530
  num of homozygotes: 0
population: African
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

19-36505157-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36505157
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36505157
    reference: chr 19
allele count: 1
allele frequency: 8.332777814812346e-6
allele num: 120008
alternate allele: G
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12988
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11422
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1891
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16344
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1199
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7058
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3710
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3147
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2744
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2586
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11480
  num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 193
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5072
bin: 1.75e1
variant carriers: 3

GenotypeDepth
all individuals: 12853
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4656
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2598
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1500
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 336
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4530
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1206
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8605
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 655
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16102
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 464
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 999
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1709
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3431
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2211
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3369
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2058
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2184
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6878
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1326
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16541
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2501
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1828
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9146
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 4346
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11264
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.124823911312549e-5
allele num: 65308
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.916198262646909e-4
allele num: 15656
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.231e0

MQRankSum
type: SiteQuality
SIO_000300: 5.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.45e-1

DP
type: SiteQuality
SIO_000300: 1.712769e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

QD
type: SiteQuality
SIO_000300: 1.36e1

FS
type: SiteQuality
SIO_000300: 5.531e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

GenotypeDepth
all individuals: 1142
bin: 7.5e0
variant carriers: 27

GenotypeDepth
all individuals: 4971
bin: 1.75e1
variant carriers: 393

GenotypeDepth
all individuals: 315
bin: 6.75e1
variant carriers: 38

GenotypeDepth
all individuals: 135
bin: 8.25e1
variant carriers: 15

GenotypeDepth
all individuals: 15805
bin: 2.25e1
variant carriers: 558

GenotypeDepth
all individuals: 8745
bin: 3.25e1
variant carriers: 640

GenotypeDepth
all individuals: 4778
bin: 3.75e1
variant carriers: 518

GenotypeDepth
all individuals: 4309
bin: 1.25e1
variant carriers: 164

GenotypeDepth
all individuals: 78
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 488
bin: 6.25e1
variant carriers: 57

GenotypeDepth
all individuals: 2747
bin: 4.25e1
variant carriers: 378

GenotypeDepth
all individuals: 1065
bin: 5.25e1
variant carriers: 154

GenotypeDepth
all individuals: 92
bin: 9.25e1
variant carriers: 12

GenotypeDepth
all individuals: 1612
bin: 4.75e1
variant carriers: 269

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 7

GenotypeDepth
all individuals: 696
bin: 5.75e1
variant carriers: 90

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 25

GenotypeDepth
all individuals: 12827
bin: 2.75e1
variant carriers: 650

GenotypeDepth
all individuals: 195
bin: 7.75e1
variant carriers: 17

GenotypeDepth
all individuals: 348
bin: 9.75e1
variant carriers: 37

GenotypeQuality
all individuals: 2067
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2296
bin: 3.75e1
variant carriers: 10

GenotypeQuality
all individuals: 4048
bin: 7.75e1
variant carriers: 17

GenotypeQuality
all individuals: 3223
bin: 7.25e1
variant carriers: 15

GenotypeQuality
all individuals: 442
bin: 5.75e1
variant carriers: 8

GenotypeQuality
all individuals: 120
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 2033
bin: 9.25e1
variant carriers: 17

GenotypeQuality
all individuals: 1651
bin: 4.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1263
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 15738
bin: 6.25e1
variant carriers: 19

GenotypeQuality
all individuals: 163
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 3099
bin: 8.25e1
variant carriers: 21

GenotypeQuality
all individuals: 1266
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1930
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 12075
bin: 9.75e1
variant carriers: 3869

GenotypeQuality
all individuals: 126
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 944
bin: 5.25e1
variant carriers: 12

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6499
bin: 6.75e1
variant carriers: 23

GenotypeQuality
all individuals: 1598
bin: 8.75e1
variant carriers: 10

East Asian
type: Population
allele count: 1540
allele frequency: 1.826809015421115e-1
allele num: 8430
num of homozygotes: 142

African
type: Population
allele count: 419
allele frequency: 4.115105087409154e-2
allele num: 10182
num of homozygotes: 13

Latino
type: Population
allele count: 441
allele frequency: 3.92418579818473e-2
allele num: 11238
num of homozygotes: 7

Other
type: Population
allele count: 16
allele frequency: 1.818181818181818e-2
allele num: 880
num of homozygotes: 0

South Asian
type: Population
allele count: 1720
allele frequency: 1.097218678234243e-1
allele num: 15676
num of homozygotes: 107

European (Non-Finnish)
type: Population
allele count: 142
allele frequency: 2.174445669484258e-3
allele num: 65304
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.095702529716549e-4
allele num: 6562
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

QD
type: SiteQuality
SIO_000300: 1.796e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.39e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

DP
type: SiteQuality
SIO_000300: 1.733339e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.426e0

FS
type: SiteQuality
SIO_000300: 1.912e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.08e-1

GenotypeDepth
all individuals: 4192
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 131
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1580
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4834
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2709
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8884
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15950
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1124
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1046
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 682
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13063
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 247
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4665
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2253
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1307
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1767
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2107
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2275
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3466
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9198
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1266
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4477
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3433
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1655
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6963
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16224
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.063631628932937e-5
allele num: 65282
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11272
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

DP
type: SiteQuality
SIO_000300: 1.734782e6

VQSLOD
type: SiteQuality
SIO_000300: 5.649999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

FS
type: SiteQuality
SIO_000300: 1.683e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.483e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.89e-1

GenotypeDepth
all individuals: 5133
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1637
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1395
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1060
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 197
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14863
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 808
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19304
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 131
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 670
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2845
bin: 4.25e1
variant carriers: 4

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10375
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4923
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9278
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 185
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8075
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22643
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3760
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1924
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3817
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.361944251081989e-4
allele num: 66082
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.947798987144527e-4
allele num: 10268
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15922
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

FS
type: SiteQuality
SIO_000300: 3.134e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
SIO_000300: 1.823034e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.063e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.18e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.524e1

GenotypeDepth
all individuals: 737
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10387
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 687
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 636
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 131
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2847
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1641
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5147
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 19415
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 249
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1317
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1061
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14905
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4952
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1918
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3756
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2415
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22759
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3825
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9273
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 444
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512310205069264e-5
allele num: 66124
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.675e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e0

FS
type: SiteQuality
SIO_000300: 1.232e0

MQRankSum
type: SiteQuality
SIO_000300: -3.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.16e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 1.759e1

DP
type: SiteQuality
SIO_000300: 1.825194e6

GenotypeDepth
all individuals: 5180
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 563
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 619
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1060
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1096
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2870
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 691
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19535
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1649
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10483
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15036
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 485
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4964
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23221
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3839
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3757
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1914
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8177
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9284
bin: 9.75e1
variant carriers: 5

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.554467712204998e-5
allele num: 66186
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16028
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-2

DP
type: SiteQuality
SIO_000300: 1.83215e6

VQSLOD
type: SiteQuality
SIO_000300: 2.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.169e0

QD
type: SiteQuality
SIO_000300: 1.494e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.48e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.07e-1

GenotypeDepth
all individuals: 341
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2893
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 249
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 691
bin: 5.75e1
variant carriers: 2

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

GenotypeDepth
all individuals: 309
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1656
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19889
bin: 2.25e1
variant carriers: 4

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15662
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 132
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 449
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 197
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5237
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5032
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8349
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 167
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3780
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1929
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9303
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 3912
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24547
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 481
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.258355916892502e-4
allele num: 66420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16220
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

DP
type: SiteQuality
SIO_000300: 1.850802e6

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

QD
type: SiteQuality
SIO_000300: 1.371e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeDepth
all individuals: 1658
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10722
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15912
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 691
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 206
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 488
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 132
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2885
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1063
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5226
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8429
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 282
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9293
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3914
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5015
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3777
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25207
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.74e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.147e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.461e1

DP
type: SiteQuality
SIO_000300: 1.857381e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

GenotypeDepth
all individuals: 179
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10740
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5224
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1655
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1063
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20090
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2883
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9292
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 3919
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5024
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2437
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8438
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25240
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3776
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004807692307692e-5
allele num: 66560
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.44e-1

FS
type: SiteQuality
SIO_000300: 1.303e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

DP
type: SiteQuality
SIO_000300: 1.858474e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

QD
type: SiteQuality
SIO_000300: 1.103e1

GenotypeDepth
all individuals: 2886
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 20087
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5226
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16049
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1656
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10764
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 51
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25373
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8444
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5018
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9293
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3919
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1930
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3778
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2435
bin: 9.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66576
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.984e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.37e-1

QD
type: SiteQuality
SIO_000300: 6.34e0

VQSLOD
type: SiteQuality
SIO_000300: -1.444e0

MQRankSum
type: SiteQuality
SIO_000300: -1.092e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.860164e6

GenotypeDepth
all individuals: 2882
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10776
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 135
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20077
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16126
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1654
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 488
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1064
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3772
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2433
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1929
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5018
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3921
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9292
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 8457
bin: 6.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.861443e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

MQRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.517e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.495e0

GenotypeDepth
all individuals: 5225
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1655
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2880
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10772
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1063
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 488
bin: 6.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 249
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 689
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20075
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25502
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1930
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8465
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3774
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3925
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5018
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9295
bin: 9.75e1
variant carriers: 3

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.593360995850622e-4
allele num: 11568
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 1.378e0

DP
type: SiteQuality
SIO_000300: 1.861896e6

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.72e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.006e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.356e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

GenotypeDepth
all individuals: 689
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16158
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5225
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20075
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1655
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 249
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1063
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 488
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2880
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10772
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1930
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3925
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5018
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3774
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9295
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8465
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25502
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50154659299078e-5
allele num: 66598
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.72e-1

DP
type: SiteQuality
SIO_000300: 1.861896e6

FS
type: SiteQuality
SIO_000300: 1.378e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.356e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.006e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-1

GenotypeDepth
all individuals: 16242
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 10791
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2881
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 20086
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1654
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5229
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1064
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 344
bin: 9.75e1
variant carriers: 5

GenotypeDepth
all individuals: 109
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25652
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5019
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3774
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3926
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2434
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1929
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9302
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8478
bin: 6.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 9
allele frequency: 8.688936088047886e-4
allele num: 10358
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.225e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.815e0

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

DP
type: SiteQuality
SIO_000300: 1.86428e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 5229
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 691
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2883
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 75
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10795
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16243
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20083
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1655
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1064
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8478
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9296
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3924
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 98
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2437
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 3774
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1929
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25660
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5020
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.171e0

FS
type: SiteQuality
SIO_000300: 6.809e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.114e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.37e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.235e0

QD
type: SiteQuality
SIO_000300: 1.731e1

DP
type: SiteQuality
SIO_000300: 1.863861e6

GenotypeDepth
all individuals: 134
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2884
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 690
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16253
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1654
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10790
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5230
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20076
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1064
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2437
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9298
bin: 9.75e1
variant carriers: 3

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

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

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

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

GenotypeQuality
all individuals: 105
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25655
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5022
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3925
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3774
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1929
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8474
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.43e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.098e0

FS
type: SiteQuality
SIO_000300: 5.101e0

VQSLOD
type: SiteQuality
SIO_000300: 3.63e-1

DP
type: SiteQuality
SIO_000300: 1.864006e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.92e-1

QD
type: SiteQuality
SIO_000300: 1.122e1

GenotypeDepth
all individuals: 1655
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10787
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5232
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16259
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20068
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2883
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 340
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 691
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3924
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3773
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1929
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 108
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9297
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 25655
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2437
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8472
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5020
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.64e-1

FS
type: SiteQuality
SIO_000300: 7.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

QD
type: SiteQuality
SIO_000300: 8.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.78e-1

DP
type: SiteQuality
SIO_000300: 1.863978e6

GenotypeDepth
all individuals: 5229
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 10793
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20053
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1654
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2883
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16262
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1929
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3922
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3772
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25667
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8467
bin: 6.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 5017
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9297
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2437
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

DP
type: SiteQuality
SIO_000300: 1.863785e6

MQRankSum
type: SiteQuality
SIO_000300: -8.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.405e0

QD
type: SiteQuality
SIO_000300: 1.036e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.753e-1

FS
type: SiteQuality
SIO_000300: 3.585e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.528e0

GenotypeDepth
all individuals: 78
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20017
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5230
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2883
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1654
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 113
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10787
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16246
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 1.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 25622
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9297
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3921
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3772
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8458
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1929
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5011
bin: 7.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.676795045480937e-5
allele num: 10334
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.863158e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.85e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

QD
type: SiteQuality
SIO_000300: 1.016e1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 4.793e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.019e-1

GenotypeDepth
all individuals: 10785
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1654
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 691
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 20015
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5229
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 341
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16251
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2884
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25628
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1929
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3773
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 153
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8456
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9298
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5009
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3921
bin: 7.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.676795045480937e-5
allele num: 10334
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.245e1

FS
type: SiteQuality
SIO_000300: 1.741e0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.8e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 1.863303e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e-1

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1656
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 16244
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19997
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2885
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5231
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10782
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8450
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3917
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2438
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25604
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5008
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3773
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1930
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9299
bin: 9.75e1
variant carriers: 3

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

South Asian
type: Population
allele count: 3
allele frequency: 1.818843215714805e-4
allele num: 16494
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.062e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.351e0

DP
type: SiteQuality
SIO_000300: 1.862843e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.53e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.103e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-2

GenotypeDepth
all individuals: 2887
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10780
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19946
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16238
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1653
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5230
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25553
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5006
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8446
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3917
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1929
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3772
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2438
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9297
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.005e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.734e0

FS
type: SiteQuality
SIO_000300: 6.691e0

DP
type: SiteQuality
SIO_000300: 1.862175e6

VQSLOD
type: SiteQuality
SIO_000300: -8.262e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.51e0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1653
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16222
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 10779
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19882
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5231
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2886
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 259
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3771
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8441
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25480
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5004
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9297
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1927
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3913
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502403846153846e-5
allele num: 66560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.861205e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.18e-1

QD
type: SiteQuality
SIO_000300: 6.65e0

MQRankSum
type: SiteQuality
SIO_000300: -9.409999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.039e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 9.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.539e0

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000248101
ensembl transcript: ENST00000473572
gene symbol: AC002116.8
hgvsc: ENST00000473572.2:n.64T>C

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16154
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 419
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1653
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2890
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19533
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 195
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 263
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5230
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 10768
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25053
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9297
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1926
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 130
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3902
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8401
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3768
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5000
bin: 7.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504438092372499e-5
allele num: 66470
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.091e0

FS
type: SiteQuality
SIO_000300: 3.368e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

MQ
type: SiteQuality
SIO_000300: 5.896e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.751e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.72e-1

DP
type: SiteQuality
SIO_000300: 1.856517e6

GenotypeDepth
all individuals: 5234
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1066
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 310
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 10753
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 714
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19182
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15977
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1654
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2895
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 195
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 208
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1926
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9299
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24436
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8337
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4989
bin: 7.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.519433564326604e-5
allele num: 66380
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.811e0

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.79e-1

DP
type: SiteQuality
SIO_000300: 1.850714e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
type: SiteQuality
SIO_000300: 7.45e0

MQRankSum
type: SiteQuality
SIO_000300: -4.53e0

MQ
type: SiteQuality
SIO_000300: 5.102e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 575
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1654
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15761
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10690
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5231
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2887
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 434
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18556
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 195
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23570
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9295
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4976
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3763
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1927
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3880
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8260
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16180
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508750754375377e-5
allele num: 66280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 2.187e0

VQSLOD
type: SiteQuality
SIO_000300: -5.286999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.76e-1

DP
type: SiteQuality
SIO_000300: 1.840915e6

QD
type: SiteQuality
SIO_000300: 1.719e1

MQ
type: SiteQuality
SIO_000300: 5.984e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.68e-1

GenotypeDepth
all individuals: 1654
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 469
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1066
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18157
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15618
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10656
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2887
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23021
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4973
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9296
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8199
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3874
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.673026886383348e-5
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66246
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16106
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.082e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 6.068e0

VQSLOD
type: SiteQuality
SIO_000300: -1.812e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.67e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.022e0

QD
type: SiteQuality
SIO_000300: 1.607e1

DP
type: SiteQuality
SIO_000300: 1.83508e6

GenotypeDepth
all individuals: 310
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1654
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15626
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10628
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 477
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1511
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5231
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 833
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18155
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2885
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1066
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4971
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3873
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 104
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9299
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 461
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8203
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1927
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3759
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 4
allele frequency: 3.46860908775581e-4
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16136
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66256
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.252e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 1.216e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.834748e6

FS
type: SiteQuality
SIO_000300: 2.713e0

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeDepth
all individuals: 10587
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 525
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2885
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17125
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5228
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1655
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15119
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1949
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1067
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21387
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1927
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1473
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8050
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3849
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4971
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9299
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 240
bin: 4.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.75800156128025e-5
allele num: 10248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66178
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16022
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.49e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.457e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.057e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

MQRankSum
type: SiteQuality
SIO_000300: -6.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.821143e6

GenotypeDepth
all individuals: 10429
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 352
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 336
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1144
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3238
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1966
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 639
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 523
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 743
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14345
bin: 2.75e1
variant carriers: 2

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

GenotypeDepth
all individuals: 2934
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7828
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1339
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1547
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1900
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3700
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9741
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19274
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3780
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15844
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.028467595396729e-5
allele num: 66040
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.08e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.455e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

DP
type: SiteQuality
SIO_000300: 1.821086e6

VQSLOD
type: SiteQuality
SIO_000300: 6.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

GenotypeDepth
all individuals: 16201
bin: 2.25e1
variant carriers: 14

GenotypeDepth
all individuals: 743
bin: 5.75e1
variant carriers: 58

GenotypeDepth
all individuals: 1144
bin: 5.25e1
variant carriers: 79

GenotypeDepth
all individuals: 1966
bin: 1.25e1
variant carriers: 3

GenotypeDepth
all individuals: 2934
bin: 4.25e1
variant carriers: 61

GenotypeDepth
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 523
bin: 6.25e1
variant carriers: 38

GenotypeDepth
all individuals: 207
bin: 7.75e1
variant carriers: 13

GenotypeDepth
all individuals: 10429
bin: 3.25e1
variant carriers: 39

GenotypeDepth
all individuals: 5225
bin: 3.75e1
variant carriers: 50

GenotypeDepth
all individuals: 88
bin: 9.25e1
variant carriers: 3

GenotypeDepth
all individuals: 336
bin: 6.75e1
variant carriers: 32

GenotypeDepth
all individuals: 268
bin: 7.25e1
variant carriers: 21

GenotypeDepth
all individuals: 145
bin: 8.25e1
variant carriers: 12

GenotypeDepth
all individuals: 352
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 139
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3780
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7828
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1547
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9741
bin: 9.75e1
variant carriers: 550

GenotypeQuality
all individuals: 1339
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19274
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1900
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3700
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.665657177468201e-4
allele num: 66040
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.475842891901286e-4
allele num: 11508
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 535
allele frequency: 6.206496519721578e-2
allele num: 8620
num of homozygotes: 14

South Asian
type: Population
allele count: 15
allele frequency: 9.467306235799041e-4
allele num: 15844
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.956181533646322e-4
allele num: 10224
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.17e0

QD
type: SiteQuality
SIO_000300: 1.455e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.08e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

DP
type: SiteQuality
SIO_000300: 1.821086e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

GenotypeDepth
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1722
bin: 4.75e1
variant carriers: 5

GenotypeDepth
all individuals: 10433
bin: 3.25e1
variant carriers: 4

GenotypeDepth
all individuals: 1993
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 134
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 655
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3215
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14428
bin: 2.75e1
variant carriers: 4

GenotypeDepth
all individuals: 344
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16168
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 87
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1095
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 713
bin: 5.75e1
variant carriers: 3

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 302
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 128
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3787
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9444
bin: 9.75e1
variant carriers: 44

GenotypeQuality
all individuals: 636
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1920
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4938
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19466
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3753
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7865
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2451
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 25
allele frequency: 3.784438389343022e-3
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.242152466367713e-3
allele num: 892
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.726859566732314e-4
allele num: 66010
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.56e-1

DP
type: SiteQuality
SIO_000300: 1.816008e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.825e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 1.364e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.97e0

GenotypeDepth
all individuals: 5320
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2943
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3158
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 711
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 344
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16259
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14356
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1099
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10385
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16470
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3750
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7709
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4931
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3763
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2456
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1271
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1917
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9426
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1699
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.318034306907742e-4
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65938
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.057e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.644e0

MQRankSum
type: SiteQuality
SIO_000300: 6.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

DP
type: SiteQuality
SIO_000300: 1.814062e6

GenotypeDepth
all individuals: 1900
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9701
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 932
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2569
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 611
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1533
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14775
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4250
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8552
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14655
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18574
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5085
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2204
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.411731e6

FS
type: SiteQuality
SIO_000300: 1.962e0

MQ
type: SiteQuality
SIO_000300: 5.929e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 1.986e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.524e0

GenotypeDepth
all individuals: 403
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14778
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1900
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 116
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 9700
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13764
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 611
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1534
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2204
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8545
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4250
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18574
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5092
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14657
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3798
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.95e-1

DP
type: SiteQuality
SIO_000300: 2.411895e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

QD
type: SiteQuality
SIO_000300: 1.791e1

FS
type: SiteQuality
SIO_000300: 2.781e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

VQSLOD
type: SiteQuality
SIO_000300: 8.93e-1

GenotypeDepth
all individuals: 6450
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 73
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13766
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 612
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2725
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1533
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9717
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 932
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1900
bin: 9.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 8581
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4255
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2211
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5099
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3821
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18719
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14673
bin: 9.75e1
variant carriers: 1

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.94e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.244e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.16e-1

QD
type: SiteQuality
SIO_000300: 1.095e1

DP
type: SiteQuality
SIO_000300: 2.414372e6

FS
type: SiteQuality
SIO_000300: 5.511e0

GenotypeDepth
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13768
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1533
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9718
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4272
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 612
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1900
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3821
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 14670
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8583
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18732
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2210
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4254
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3130
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.857e1

FS
type: SiteQuality
SIO_000300: 4.488e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.329e0

QD
type: SiteQuality
SIO_000300: 1.41e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.91e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

DP
type: SiteQuality
SIO_000300: 2.41448e6

GenotypeDepth
all individuals: 1534
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 932
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 405
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 230
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14832
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1902
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 161
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2570
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 612
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3819
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5106
bin: 7.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 2214
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18736
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8584
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14669
bin: 9.75e1
variant carriers: 7

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 5.767012687427913e-4
allele num: 10404
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.258e0

DP
type: SiteQuality
SIO_000300: 2.415004e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 1.376e1

FS
type: SiteQuality
SIO_000300: 1.165e0

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

MQ
type: SiteQuality
SIO_000300: 5.923e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-1

GenotypeDepth
all individuals: 2570
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 931
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 611
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2705
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4274
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6463
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9727
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13784
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 229
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4256
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18724
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 14665
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3818
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3132
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5103
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8589
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2215
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.661e0

FS
type: SiteQuality
SIO_000300: 7.81e-1

MQ
type: SiteQuality
SIO_000300: 5.787e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.674e0

QD
type: SiteQuality
SIO_000300: 1.394e1

DP
type: SiteQuality
SIO_000300: 2.414764e6

GenotypeDepth
all individuals: 931
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 611
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6466
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1534
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2572
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9724
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 229
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2215
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18767
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5098
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8586
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3817
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14668
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3130
bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.414951e6

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.732e0

MQ
type: SiteQuality
SIO_000300: 6.021e1

QD
type: SiteQuality
SIO_000300: 1.558e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.418e0

VQSLOD
type: SiteQuality
SIO_000300: 2.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

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

GenotypeDepth
all individuals: 404
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 611
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2578
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4277
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6469
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 931
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14854
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13798
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9725
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2708
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1901
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 229
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18779
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5091
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3822
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4263
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14668
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2221
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8600
bin: 6.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.892e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.496e1

FS
type: SiteQuality
SIO_000300: 2.578e0

MQ
type: SiteQuality
SIO_000300: 5.762e1

DP
type: SiteQuality
SIO_000300: 2.416091e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.24e-1

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

GenotypeDepth
all individuals: 230
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9723
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1535
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14855
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1900
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4279
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 932
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13806
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2705
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3129
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18809
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4262
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5092
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14669
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 8608
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3821
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.762e0

DP
type: SiteQuality
SIO_000300: 2.416231e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -6.235000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

QD
type: SiteQuality
SIO_000300: 9.34e0

GenotypeDepth
all individuals: 933
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 610
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 2685
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4277
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1899
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 229
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14671
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3820
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4263
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8603
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5093
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18775
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

VQSLOD
type: SiteQuality
SIO_000300: -2.603e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.96e-1

DP
type: SiteQuality
SIO_000300: 2.416113e6

QD
type: SiteQuality
SIO_000300: 2.502e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

GenotypeDepth
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 227
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2580
bin: 5.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 9720
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 608
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 933
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6474
bin: 4.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3822
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8606
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18787
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5092
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4263
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14670
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.42512428761974e-4
allele num: 16494
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

DP
type: SiteQuality
SIO_000300: 2.416251e6

MQRankSum
type: SiteQuality
SIO_000300: -5.19e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 9.57e0

FS
type: SiteQuality
SIO_000300: 1.752e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.391e0

GenotypeDepth
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1535
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 227
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4278
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14855
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 608
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13816
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2685
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1901
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 175
bin: 8.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2219
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14670
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 5092
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8606
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3822
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4263
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18787
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21256214380987e-4
allele num: 16494
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -5.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.391e0

QD
type: SiteQuality
SIO_000300: 9.57e0

VQSLOD
type: SiteQuality
SIO_000300: 4.95e-1

FS
type: SiteQuality
SIO_000300: 1.752e0

DP
type: SiteQuality
SIO_000300: 2.416251e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

GenotypeDepth
all individuals: 1535
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2579
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6471
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 608
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14848
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5095
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3129
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18792
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4258
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8607
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14659
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3819
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.311e0

FS
type: SiteQuality
SIO_000300: 8.84e-1

QD
type: SiteQuality
SIO_000300: 1.124e1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.415695e6

GenotypeDepth
all individuals: 227
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1900
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2676
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 608
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9722
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2219
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3820
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5095
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14659
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18769
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8603
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4260
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 2.69e0

DP
type: SiteQuality
SIO_000300: 2.415453e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 1.282e1

MQRankSum
type: SiteQuality
SIO_000300: -8.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 177
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4238
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5049
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18422
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2213
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14535
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999490086685263e-5
allele num: 66678
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.055e0

MQ
type: SiteQuality
SIO_000300: 5.849e1

DP
type: SiteQuality
SIO_000300: 2.411657e6

MQRankSum
type: SiteQuality
SIO_000300: -7.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.048e1

FS
type: SiteQuality
SIO_000300: 4.4113e1

QD
type: SiteQuality
SIO_000300: 1.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

GenotypeDepth
all individuals: 14718
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5049
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 14535
bin: 9.75e1
variant carriers: 49

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 4238
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 200
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 18422
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 8511
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2213
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 34
allele frequency: 5.216324025774778e-3
allele num: 6518
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 8.670520231213873e-4
allele num: 10380
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 3.899337112690842e-4
allele num: 66678
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.4113e1

VQSLOD
type: SiteQuality
SIO_000300: -1.048e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.055e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.849e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQRankSum
type: SiteQuality
SIO_000300: -7.45e-1

DP
type: SiteQuality
SIO_000300: 2.411657e6

QD
type: SiteQuality
SIO_000300: 1.61e0

GenotypeQuality
all individuals: 84
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 236
bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 73
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 2985
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 18056
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 3652
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2109
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 4869
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8265
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 383
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 346
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4103
bin: 8.25e1
variant carriers: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 82
allele frequency: 1.238521024649589e-3
allele num: 66208
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 58
allele frequency: 9.382076997735361e-3
allele num: 6182
num of homozygotes: 0

African
type: Population
allele count: 44
allele frequency: 4.287663223543169e-3
allele num: 10262
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 5.9161e1

MQ
type: SiteQuality
SIO_000300: 5.892e1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.731e0

VQSLOD
type: SiteQuality
SIO_000300: -1.712e1

DP
type: SiteQuality
SIO_000300: 2.403485e6

GenotypeQuality
all individuals: 291
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18475
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3067
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5006
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.256e0

MQ
type: SiteQuality
SIO_000300: 5.905e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.208e0

FS
type: SiteQuality
SIO_000300: 7.115e0

MQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.46e-1

QD
type: SiteQuality
SIO_000300: 2.831e1

DP
type: SiteQuality
SIO_000300: 2.398186e6

GenotypeQuality
all individuals: 2155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3734
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8470
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18500
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4995
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.312673450508788e-4
allele num: 8648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.396851e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.082e0

VQSLOD
type: SiteQuality
SIO_000300: 8.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.118e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 1.064e1

FS
type: SiteQuality
SIO_000300: 9.022e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.277e0

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-1

GenotypeQuality
all individuals: 17670
bin: 6.25e1
variant carriers: 20

GenotypeQuality
all individuals: 591
bin: 2.25e1
variant carriers: 23

GenotypeQuality
all individuals: 650
bin: 5.75e1
variant carriers: 15

GenotypeQuality
all individuals: 261
bin: 1.25e1
variant carriers: 13

GenotypeQuality
all individuals: 11172
bin: 9.75e1
variant carriers: 292

GenotypeQuality
all individuals: 438
bin: 4.25e1
variant carriers: 20

GenotypeQuality
all individuals: 393
bin: 3.25e1
variant carriers: 28

East Asian
type: Population
allele count: 11
allele frequency: 1.309523809523809e-3
allele num: 8400
num of homozygotes: 0

African
type: Population
allele count: 135
allele frequency: 1.497338065661047e-2
allele num: 9016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 112
allele frequency: 2.100525131282821e-2
allele num: 5332
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.220107369448512e-4
allele num: 16392
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.640776699029126e-3
allele num: 824
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 306
allele frequency: 4.92737754017584e-3
allele num: 62102
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.655337227827934e-4
allele num: 11298
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.16e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.65e-1

MQ
type: SiteQuality
SIO_000300: 5.857e1

VQSLOD
type: SiteQuality
SIO_000300: -7.759999999999999e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.589e0

FS
type: SiteQuality
SIO_000300: 1.29681e2

QD
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e0

DP
type: SiteQuality
SIO_000300: 2.373541e6

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

GenotypeQuality
all individuals: 11617
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3736
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66558
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.22753e6

MQ
type: SiteQuality
SIO_000300: 5.903e1

MQRankSum
type: SiteQuality
SIO_000300: 3.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.285e0

VQSLOD
type: SiteQuality
SIO_000300: -4.183e-1

QD
type: SiteQuality
SIO_000300: 1.702e1

GenotypeQuality
all individuals: 3731
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8975
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21493
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004807692307692e-5
allele num: 66560
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.997e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

MQ
type: SiteQuality
SIO_000300: 5.843e1

DP
type: SiteQuality
SIO_000300: 2.225353e6

MQRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.062e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.918e0

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

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21447
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11608
bin: 9.75e1
variant carriers: 1

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e0

QD
type: SiteQuality
SIO_000300: 1.323e1

MQRankSum
type: SiteQuality
SIO_000300: -1.207e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

MQ
type: SiteQuality
SIO_000300: 5.281e1

VQSLOD
type: SiteQuality
SIO_000300: -1.751e0

FS
type: SiteQuality
SIO_000300: 1.0736e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.81e0

DP
type: SiteQuality
SIO_000300: 2.223909e6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504573904670197e-5
allele num: 66464
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

FS
type: SiteQuality
SIO_000300: 2.91e0

QD
type: SiteQuality
SIO_000300: 1.066e1

MQ
type: SiteQuality
SIO_000300: 5.931e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.005e0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 2.206083e6

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 9.41e0

FS
type: SiteQuality
SIO_000300: 2.921e0

MQRankSum
type: SiteQuality
SIO_000300: -1.373e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.297e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.151e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.319e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.201809e6

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.537e0

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

MQ
type: SiteQuality
SIO_000300: 5.526e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.42e-1

DP
type: SiteQuality
SIO_000300: 2.179786e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.027e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66348
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

DP
type: SiteQuality
SIO_000300: 2.169449e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.871e1

QD
type: SiteQuality
SIO_000300: 1.326e1

MQRankSum
type: SiteQuality
SIO_000300: -4.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.024e-1

FS
type: SiteQuality
SIO_000300: 1.496e0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.89e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.61e-1

QD
type: SiteQuality
SIO_000300: 1.201e1

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.1e-2

DP
type: SiteQuality
SIO_000300: 2.163272e6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.207729468599034e-4
allele num: 66240
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

FS
type: SiteQuality
SIO_000300: 1.386e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 2.149417e6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

DP
type: SiteQuality
SIO_000300: 2.149417e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

FS
type: SiteQuality
SIO_000300: 1.386e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.386e0

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 2.149417e6