1-44684086-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684086
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684086
    reference: chr 1
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.497G>A
  hgvsp: ENSP00000312697.5:p.Arg166His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.497G>A
  hgvsp: ENSP00000361363.2:p.Arg166His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3582G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.497G>A
  hgvsp: ENSP00000409200.1:p.Arg166His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361364
  ensembl transcript: ENST00000372290
  gene symbol: DMAP1
  hgvsc: ENST00000372290.4:c.380G>A
  hgvsp: ENSP00000361364.4:p.Arg127His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.575G>A
  hgvsp: ENSP00000402494.1:p.Arg192His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.497G>A
  hgvsp: ENSP00000401099.1:p.Arg166His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.497G>A
  hgvsp: ENSP00000354697.6:p.Arg166His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.50G>A
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3508
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7522
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg166His
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD

1-44684090-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684090
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684090
    reference: chr 1
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.501T>G
  hgvsp: ENSP00000361363.2:p.Phe167Leu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.579T>G
  hgvsp: ENSP00000402494.1:p.Phe193Leu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3586T>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.54T>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.501T>G
  hgvsp: ENSP00000409200.1:p.Phe167Leu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.501T>G
  hgvsp: ENSP00000312697.5:p.Phe167Leu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.501T>G
  hgvsp: ENSP00000401099.1:p.Phe167Leu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361364
  ensembl transcript: ENST00000372290
  gene symbol: DMAP1
  hgvsc: ENST00000372290.4:c.384T>G
  hgvsp: ENSP00000361364.4:p.Phe128Leu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.501T>G
  hgvsp: ENSP00000354697.6:p.Phe167Leu
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40524
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Phe167Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

1-44684093-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684093
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684093
    reference: chr 1
allele count: 10
allele frequency: 8.23641814647646e-5
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.582C>G
  hgvsp: ENSP00000402494.1:p.Asp194Glu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361364
  ensembl transcript: ENST00000372290
  gene symbol: DMAP1
  hgvsc: ENST00000372290.4:c.387C>G
  hgvsp: ENSP00000361364.4:p.Asp129Glu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.57C>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.504C>G
  hgvsp: ENSP00000354697.6:p.Asp168Glu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.504C>G
  hgvsp: ENSP00000312697.5:p.Asp168Glu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.504C>G
  hgvsp: ENSP00000361363.2:p.Asp168Glu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.504C>G
  hgvsp: ENSP00000409200.1:p.Asp168Glu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.504C>G
  hgvsp: ENSP00000401099.1:p.Asp168Glu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3589C>G
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp168Glu
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

1-44684098-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684098
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684098
    reference: chr 1
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.509G>A
  hgvsp: ENSP00000409200.1:p.Arg170His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.509G>A
  hgvsp: ENSP00000354697.6:p.Arg170His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.509G>A
  hgvsp: ENSP00000361363.2:p.Arg170His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361364
  ensembl transcript: ENST00000372290
  gene symbol: DMAP1
  hgvsc: ENST00000372290.4:c.392G>A
  hgvsp: ENSP00000361364.4:p.Arg131His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3594G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.587G>A
  hgvsp: ENSP00000402494.1:p.Arg196His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.509G>A
  hgvsp: ENSP00000312697.5:p.Arg170His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.509G>A
  hgvsp: ENSP00000401099.1:p.Arg170His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.62G>A
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg170His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

1-44684100-TTTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684100
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684097
    reference: chr 1
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.517_519delGTT
  hgvsp: ENSP00000354697.6:p.Val173del
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3602_3604delGTT
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361364
  ensembl transcript: ENST00000372290
  gene symbol: DMAP1
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.517_519delGTT
  hgvsp: ENSP00000361363.2:p.Val173del
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.517_519delGTT
  hgvsp: ENSP00000312697.5:p.Val173del
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.595_597delGTT
  hgvsp: ENSP00000402494.1:p.Val199del
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.517_519delGTT
  hgvsp: ENSP00000401099.1:p.Val173del
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.517_519delGTT
  hgvsp: ENSP00000409200.1:p.Val173del
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.70_72delGTT
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40514
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val173del
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: TTTG
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

1-44684107-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684107
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684107
    reference: chr 1
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.518T>A
  hgvsp: ENSP00000361363.2:p.Val173Asp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.518T>A
  hgvsp: ENSP00000401099.1:p.Val173Asp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.596T>A
  hgvsp: ENSP00000402494.1:p.Val199Asp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.518T>A
  hgvsp: ENSP00000354697.6:p.Val173Asp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.71T>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.518T>A
  hgvsp: ENSP00000312697.5:p.Val173Asp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3603T>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.518T>A
  hgvsp: ENSP00000409200.1:p.Val173Asp
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val173Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

1-44684116-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684116
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684116
    reference: chr 1
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3612A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.605A>G
  hgvsp: ENSP00000402494.1:p.Asp202Gly
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.80A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.527A>G
  hgvsp: ENSP00000401099.1:p.Asp176Gly
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.527A>G
  hgvsp: ENSP00000409200.1:p.Asp176Gly
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.527A>G
  hgvsp: ENSP00000361363.2:p.Asp176Gly
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.527A>G
  hgvsp: ENSP00000354697.6:p.Asp176Gly
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.527A>G
  hgvsp: ENSP00000312697.5:p.Asp176Gly
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5371
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1804
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2808
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40501
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp176Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

1-44684118-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684118
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684118
    reference: chr 1
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.529C>T
  hgvsp: ENSP00000401099.1:p.Arg177Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.607C>T
  hgvsp: ENSP00000402494.1:p.Arg203Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.529C>T
  hgvsp: ENSP00000409200.1:p.Arg177Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.529C>T
  hgvsp: ENSP00000312697.5:p.Arg177Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.529C>T
  hgvsp: ENSP00000354697.6:p.Arg177Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.82C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3614C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.529C>T
  hgvsp: ENSP00000361363.2:p.Arg177Trp
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1804
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg177Trp
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-44684126-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684126
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684126
    reference: chr 1
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.90C>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3622C>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.615C>A
  hgvsp: ENSP00000402494.1:p.Asp205Glu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.537C>A
  hgvsp: ENSP00000361363.2:p.Asp179Glu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.537C>A
  hgvsp: ENSP00000354697.6:p.Asp179Glu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.537C>A
  hgvsp: ENSP00000312697.5:p.Asp179Glu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.537C>A
  hgvsp: ENSP00000409200.1:p.Asp179Glu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.537C>A
  hgvsp: ENSP00000401099.1:p.Asp179Glu
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp179Glu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-44684129-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684129
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684129
    reference: chr 1
allele count: 4
allele frequency: 3.295001482750667e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.93C>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3625C>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.540C>A
  hgvsp: ENSP00000409200.1:p.His180Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.540C>A
  hgvsp: ENSP00000312697.5:p.His180Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.540C>A
  hgvsp: ENSP00000361363.2:p.His180Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.540C>A
  hgvsp: ENSP00000401099.1:p.His180Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.540C>A
  hgvsp: ENSP00000354697.6:p.His180Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.618C>A
  hgvsp: ENSP00000402494.1:p.His206Gln
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3508
  bin: 7.75e1
  variant carriers: 0
hgvs: p.His180Gln
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

1-44684129-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684129
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684129
    reference: chr 1
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.540C>T
  hgvsp: ENST00000372289.2:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.540C>T
  hgvsp: ENST00000440641.1:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.540C>T
  hgvsp: ENST00000361745.6:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.540C>T
  hgvsp: ENST00000315913.5:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.540C>T
  hgvsp: ENST00000446292.1:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.618C>T
  hgvsp: ENST00000437511.1:c.618C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3625C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.93C>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7513
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2808
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His180His
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ

1-44684132-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684132
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684132
    reference: chr 1
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.543G>A
  hgvsp: ENST00000315913.5:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.621G>A
  hgvsp: ENST00000437511.1:c.621G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.543G>A
  hgvsp: ENST00000440641.1:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.543G>A
  hgvsp: ENST00000446292.1:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.543G>A
  hgvsp: ENST00000372289.2:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3628G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.543G>A
  hgvsp: ENST00000361745.6:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.96G>A
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7510
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1809
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln181Gln
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

1-44684150-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684150
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684150
    reference: chr 1
allele count: 2
allele frequency: 1.648206751054852e-5
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.552+9T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.552+9T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.552+9T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3637+9T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.552+9T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.105+9T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.552+9T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.630+9T>C
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40278
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

1-44684157-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684157
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684157
    reference: chr 1
allele count: 6
allele frequency: 4.945843018942579e-5
allele num: 121314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3637+16T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.552+16T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.552+16T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.105+16T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.630+16T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.552+16T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.552+16T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.552+16T>C
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

1-44684158-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684158
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684158
    reference: chr 1
allele count: 36
allele frequency: 2.967456889445745e-4
allele num: 121316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.552+17T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.630+17T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.105+17T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.552+17T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.552+17T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.552+17T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.552+17T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3637+17T>C
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39999
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

1-44684162-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684162
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684162
    reference: chr 1
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.552+21A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.630+21A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.552+21A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.552+21A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.552+21A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.105+21A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.552+21A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3637+21A>G
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3492
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7430
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

1-44684165-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684165
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684165
    reference: chr 1
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.552+24G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.552+24G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.552+24G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.552+24G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.552+24G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.105+24G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.630+24G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3637+24G>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7427
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39618
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

1-44684173-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684173
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684173
    reference: chr 1
allele count: 2
allele frequency: 1.649593375233005e-5
allele num: 121242
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.552+32G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.552+32G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.552+32G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.552+32G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.630+32G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.105+32G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.552+32G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3637+32G>A
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2399
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2778
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

1-44684186-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684186
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684186
    reference: chr 1
allele count: 1
allele frequency: 8.255184255712587e-6
allele num: 121136
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.552+45G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.552+45G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3637+45G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.552+45G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.552+45G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.630+45G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.552+45G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.105+45G>A
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37764
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7242
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2767
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS

1-44684188-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684188
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684188
    reference: chr 1
allele count: 2
allele frequency: 1.651254953764861e-5
allele num: 121120
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.552+47A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.552+47A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3637+47A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.552+47A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.552+47A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.552+47A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.105+47A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.630+47A>G
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3496
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

1-44684188-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684188
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684188
    reference: chr 1
allele count: 1
allele frequency: 8.256274768824306e-6
allele num: 121120
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.552+47A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.552+47A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.630+47A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.552+47A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.105+47A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.552+47A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3637+47A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.552+47A>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7254
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-44684191-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684191
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684191
    reference: chr 1
allele count: 1
allele frequency: 8.26541913940456e-6
allele num: 120986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.105+50C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.552+50C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.552+50C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.552+50C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.552+50C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.552+50C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3637+50C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.630+50C>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3493
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/1-44684215-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684215
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684214
    reference: chr 1
allele count: 4
allele frequency: 3.321541859731287e-5
allele num: 120426
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3638-44delC
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.106-44delC
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.553-44delC
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.553-44delC
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.631-44delC
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.553-44delC
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.553-44delC
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.553-44delC
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6644
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9198
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14893
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3567
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4563
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: AC
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

1-44684219-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684219
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684219
    reference: chr 1
allele count: 1
allele frequency: 8.30827005200977e-6
allele num: 120362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.553-41G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.106-41G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.553-41G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.631-41G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.553-41G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.553-41G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.553-41G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3638-41G>A
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2159
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

1-44684225-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684225
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684225
    reference: chr 1
allele count: 3
allele frequency: 2.493226734039193e-5
allele num: 120326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.553-35G>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.553-35G>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.553-35G>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3638-35G>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.553-35G>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.106-35G>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.553-35G>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.631-35G>C
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7269
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2153
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15624
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

1-44684227-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684227
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684227
    reference: chr 1
allele count: 1
allele frequency: 8.310341388824253e-6
allele num: 120332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.553-33A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.553-33A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.631-33A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.553-33A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.553-33A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.553-33A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.106-33A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3638-33A>G
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9168
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3306
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3562
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-44684241-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684241
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684241
    reference: chr 1
allele count: 1
allele frequency: 8.30827005200977e-6
allele num: 120362
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.553-19A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3638-19A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.553-19A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.553-19A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.106-19A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.553-19A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.631-19A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.553-19A>G
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

1-44684243-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684243
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684243
    reference: chr 1
allele count: 1
allele frequency: 8.310203267571925e-6
allele num: 120334
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.553-17C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.553-17C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.631-17C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.553-17C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.106-17C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.553-17C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.553-17C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3638-17C>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6625
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2148
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7277
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5005
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3558
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3295
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
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: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

1-44684251-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684251
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684251
    reference: chr 1
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.553-9G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.553-9G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.631-9G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.553-9G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.106-9G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.553-9G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.553-9G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3638-9G>A
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13009
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4539
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3557
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

1-44684253-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684253
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684253
    reference: chr 1
allele count: 3
allele frequency: 2.490411914130597e-5
allele num: 120462
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.553-7T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.106-7T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.553-7T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3638-7T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.553-7T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.553-7T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.553-7T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.631-7T>C
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4541
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16288
  bin: 6.25e1
  variant carriers: 0
hgvs: c.553-7T>C
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-44684255-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684255
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684255
    reference: chr 1
allele count: 1
allele frequency: 8.301235223801302e-6
allele num: 120464
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.553-5C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3638-5C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.553-5C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.106-5C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.553-5C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.553-5C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.631-5C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.553-5C>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4537
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7308
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: c.553-5C>T
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

1-44684262-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684262
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684262
    reference: chr 1
allele count: 1
allele frequency: 8.295450774795103e-6
allele num: 120548
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.555G>T
  hgvsp: ENSP00000312697.5:p.Lys185Asn
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.108G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.555G>T
  hgvsp: ENSP00000361363.2:p.Lys185Asn
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.555G>T
  hgvsp: ENSP00000409200.1:p.Lys185Asn
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.555G>T
  hgvsp: ENSP00000354697.6:p.Lys185Asn
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.633G>T
  hgvsp: ENSP00000402494.1:p.Lys211Asn
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.555G>T
  hgvsp: ENSP00000401099.1:p.Lys185Asn
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3640G>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7322
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16613
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys185Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-44684263-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684263
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684263
    reference: chr 1
allele count: 1
allele frequency: 8.299995020002988e-6
allele num: 120482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.556C>T
  hgvsp: ENSP00000354697.6:p.Arg186Cys
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.556C>T
  hgvsp: ENSP00000312697.5:p.Arg186Cys
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.556C>T
  hgvsp: ENSP00000401099.1:p.Arg186Cys
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3641C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.634C>T
  hgvsp: ENSP00000402494.1:p.Arg212Cys
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.556C>T
  hgvsp: ENSP00000361363.2:p.Arg186Cys
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.556C>T
  hgvsp: ENSP00000409200.1:p.Arg186Cys
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.109C>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4993
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4536
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg186Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/1-44684278-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684278
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684278
    reference: chr 1
allele count: 1
allele frequency: 8.279516476237788e-6
allele num: 120780
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.571C>A
  hgvsp: ENSP00000312697.5:p.Leu191Met
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.649C>A
  hgvsp: ENSP00000402494.1:p.Leu217Met
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.571C>A
  hgvsp: ENSP00000401099.1:p.Leu191Met
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.124C>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.571C>A
  hgvsp: ENSP00000361363.2:p.Leu191Met
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.571C>A
  hgvsp: ENSP00000409200.1:p.Leu191Met
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3656C>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.571C>A
  hgvsp: ENSP00000354697.6:p.Leu191Met
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15594
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu191Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP

1-44684284-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684284
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684284
    reference: chr 1
allele count: 1
allele frequency: 8.272803984182399e-6
allele num: 120878
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.577G>A
  hgvsp: ENSP00000312697.5:p.Glu193Lys
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.655G>A
  hgvsp: ENSP00000402494.1:p.Glu219Lys
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.577G>A
  hgvsp: ENSP00000401099.1:p.Glu193Lys
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.577G>A
  hgvsp: ENSP00000354697.6:p.Glu193Lys
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.130G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.577G>A
  hgvsp: ENSP00000361363.2:p.Glu193Lys
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3662G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.577G>A
  hgvsp: ENSP00000409200.1:p.Glu193Lys
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4530
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4992
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu193Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

1-44684284-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684284
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684284
    reference: chr 1
allele count: 1
allele frequency: 8.272803984182399e-6
allele num: 120878
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.577G>C
  hgvsp: ENSP00000354697.6:p.Glu193Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.577G>C
  hgvsp: ENSP00000361363.2:p.Glu193Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.655G>C
  hgvsp: ENSP00000402494.1:p.Glu219Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.130G>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.577G>C
  hgvsp: ENSP00000312697.5:p.Glu193Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.577G>C
  hgvsp: ENSP00000409200.1:p.Glu193Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3662G>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.577G>C
  hgvsp: ENSP00000401099.1:p.Glu193Gln
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18076
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu193Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

1-44684288-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684288
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684288
    reference: chr 1
allele count: 2
allele frequency: 1.653876686954221e-5
allele num: 120928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.134G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.581G>A
  hgvsp: ENSP00000354697.6:p.Arg194Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.581G>A
  hgvsp: ENSP00000312697.5:p.Arg194Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.581G>A
  hgvsp: ENSP00000361363.2:p.Arg194Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.659G>A
  hgvsp: ENSP00000402494.1:p.Arg220Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.581G>A
  hgvsp: ENSP00000409200.1:p.Arg194Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3666G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.581G>A
  hgvsp: ENSP00000401099.1:p.Arg194Gln
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3302
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18240
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7410
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15588
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4524
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg194Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

1-44684293-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684293
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684293
    reference: chr 1
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3671T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.586T>C
  hgvsp: ENSP00000361363.2:p.Tyr196His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.139T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.586T>C
  hgvsp: ENSP00000354697.6:p.Tyr196His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.664T>C
  hgvsp: ENSP00000402494.1:p.Tyr222His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.586T>C
  hgvsp: ENSP00000401099.1:p.Tyr196His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.586T>C
  hgvsp: ENSP00000312697.5:p.Tyr196His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.586T>C
  hgvsp: ENSP00000409200.1:p.Tyr196His
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4996
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4525
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2149
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Tyr196His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-44684294-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684294
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684294
    reference: chr 1
allele count: 2
allele frequency: 1.652346331791144e-5
allele num: 121040
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.140A>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.587A>C
  hgvsp: ENSP00000409200.1:p.Tyr196Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.587A>C
  hgvsp: ENSP00000354697.6:p.Tyr196Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.587A>C
  hgvsp: ENSP00000312697.5:p.Tyr196Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.665A>C
  hgvsp: ENSP00000402494.1:p.Tyr222Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.587A>C
  hgvsp: ENSP00000361363.2:p.Tyr196Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.587A>C
  hgvsp: ENSP00000401099.1:p.Tyr196Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3672A>C
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3306
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr196Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

1-44684297-ACATCTG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684297
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684291
    reference: chr 1
allele count: 1
allele frequency: 8.259275166011431e-6
allele num: 121076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.591_596delCATCTG
  hgvsp: ENSP00000409200.1:p.Ile198_Cys199del
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.591_596delCATCTG
  hgvsp: ENSP00000401099.1:p.Ile198_Cys199del
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.591_596delCATCTG
  hgvsp: ENSP00000361363.2:p.Ile198_Cys199del
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.669_674delCATCTG
  hgvsp: ENSP00000402494.1:p.Ile224_Cys225del
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.591_596delCATCTG
  hgvsp: ENSP00000312697.5:p.Ile198_Cys199del
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.144_149delCATCTG
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.591_596delCATCTG
  hgvsp: ENSP00000354697.6:p.Ile198_Cys199del
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3676_3681delCATCTG
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 13326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3554
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3308
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile198_Cys199del
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: ACATCTG
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

1-44684300-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684300
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684300
    reference: chr 1
allele count: 2
allele frequency: 1.651391297167864e-5
allele num: 121110
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.593T>C
  hgvsp: ENSP00000401099.1:p.Ile198Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3678T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.593T>C
  hgvsp: ENSP00000354697.6:p.Ile198Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.593T>C
  hgvsp: ENSP00000312697.5:p.Ile198Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.671T>C
  hgvsp: ENSP00000402494.1:p.Ile224Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.593T>C
  hgvsp: ENSP00000361363.2:p.Ile198Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.146T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.593T>C
  hgvsp: ENSP00000409200.1:p.Ile198Thr
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7448
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15583
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile198Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/1-44684309-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684309
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684309
    reference: chr 1
allele count: 5
allele frequency: 4.125616779708567e-5
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.155A>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.602A>C
  hgvsp: ENSP00000312697.5:p.Lys201Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.680A>C
  hgvsp: ENSP00000402494.1:p.Lys227Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.602A>C
  hgvsp: ENSP00000409200.1:p.Lys201Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.602A>C
  hgvsp: ENSP00000401099.1:p.Lys201Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3687A>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.602A>C
  hgvsp: ENSP00000361363.2:p.Lys201Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.602A>C
  hgvsp: ENSP00000354697.6:p.Lys201Thr
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4521
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys201Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ

1-44684318-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684318
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684318
    reference: chr 1
allele count: 3
allele frequency: 2.475043313257982e-5
allele num: 121210
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.689A>G
  hgvsp: ENSP00000402494.1:p.Asn230Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3696A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.611A>G
  hgvsp: ENSP00000361363.2:p.Asn204Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.611A>G
  hgvsp: ENSP00000409200.1:p.Asn204Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.611A>G
  hgvsp: ENSP00000401099.1:p.Asn204Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.164A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.611A>G
  hgvsp: ENSP00000312697.5:p.Asn204Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.611A>G
  hgvsp: ENSP00000354697.6:p.Asn204Ser
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7458
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3557
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn204Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

1-44684319-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684319
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684319
    reference: chr 1
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.612C>T
  hgvsp: ENST00000372289.2:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.612C>T
  hgvsp: ENST00000361745.6:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3697C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.612C>T
  hgvsp: ENST00000315913.5:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.165C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.690C>T
  hgvsp: ENST00000437511.1:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.612C>T
  hgvsp: ENST00000446292.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.612C>T
  hgvsp: ENST00000440641.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4515
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7452
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn204Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

1-44684320-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684320
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684320
    reference: chr 1
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.613G>A
  hgvsp: ENSP00000401099.1:p.Val205Met
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.166G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.613G>A
  hgvsp: ENSP00000354697.6:p.Val205Met
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.691G>A
  hgvsp: ENSP00000402494.1:p.Val231Met
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.613G>A
  hgvsp: ENSP00000312697.5:p.Val205Met
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.613G>A
  hgvsp: ENSP00000361363.2:p.Val205Met
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3698G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.613G>A
  hgvsp: ENSP00000409200.1:p.Val205Met
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4514
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4987
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3308
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7453
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val205Met
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

1-44684324-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684324
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684324
    reference: chr 1
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3702G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.617G>A
  hgvsp: ENSP00000354697.6:p.Arg206Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.617G>A
  hgvsp: ENSP00000401099.1:p.Arg206Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.170G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.617G>A
  hgvsp: ENSP00000312697.5:p.Arg206Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.695G>A
  hgvsp: ENSP00000402494.1:p.Arg232Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.617G>A
  hgvsp: ENSP00000361363.2:p.Arg206Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.617G>A
  hgvsp: ENSP00000409200.1:p.Arg206Gln
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13121
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7446
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg206Gln
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-44684327-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684327
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684327
    reference: chr 1
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.620C>G
  hgvsp: ENSP00000354697.6:p.Ala207Gly
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.620C>G
  hgvsp: ENSP00000409200.1:p.Ala207Gly
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.620C>G
  hgvsp: ENSP00000361363.2:p.Ala207Gly
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.620C>G
  hgvsp: ENSP00000401099.1:p.Ala207Gly
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.620C>G
  hgvsp: ENSP00000312697.5:p.Ala207Gly
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.173C>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.698C>G
  hgvsp: ENSP00000402494.1:p.Ala233Gly
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3705C>G
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3555
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4513
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18968
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala207Gly
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

1-44684333-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684333
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684333
    reference: chr 1
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.704C>G
  hgvsp: ENSP00000402494.1:p.Pro235Arg
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.626C>G
  hgvsp: ENSP00000312697.5:p.Pro209Arg
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.626C>G
  hgvsp: ENSP00000361363.2:p.Pro209Arg
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.179C>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.626C>G
  hgvsp: ENSP00000401099.1:p.Pro209Arg
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.626C>G
  hgvsp: ENSP00000354697.6:p.Pro209Arg
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3711C>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.626C>G
  hgvsp: ENSP00000409200.1:p.Pro209Arg
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4511
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7444
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro209Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-44684351-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684351
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684351
    reference: chr 1
allele count: 2
allele frequency: 1.650083329208125e-5
allele num: 121206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.722T>C
  hgvsp: ENSP00000402494.1:p.Ile241Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3729T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.644T>C
  hgvsp: ENSP00000312697.5:p.Ile215Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.644T>C
  hgvsp: ENSP00000361363.2:p.Ile215Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.644T>C
  hgvsp: ENSP00000354697.6:p.Ile215Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.644T>C
  hgvsp: ENSP00000401099.1:p.Ile215Thr
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.197T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.644T>C
  hgvsp: ENSP00000409200.1:p.Ile215Thr
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18970
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4982
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile215Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-44684352-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684352
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684352
    reference: chr 1
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.645A>C
  hgvsp: ENST00000446292.1:c.645A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.645A>C
  hgvsp: ENST00000315913.5:c.645A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.198A>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.645A>C
  hgvsp: ENST00000372289.2:c.645A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.723A>C
  hgvsp: ENST00000437511.1:c.723A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3730A>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.645A>C
  hgvsp: ENST00000440641.1:c.645A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.645A>C
  hgvsp: ENST00000361745.6:c.645A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13550
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2143
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7440
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3553
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile215Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/1-44684354-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684354
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684354
    reference: chr 1
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.200C>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3732C>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.647C>A
  hgvsp: ENSP00000361363.2:p.Pro216Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.647C>A
  hgvsp: ENSP00000354697.6:p.Pro216Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.725C>A
  hgvsp: ENSP00000402494.1:p.Pro242Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.647C>A
  hgvsp: ENSP00000401099.1:p.Pro216Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.647C>A
  hgvsp: ENSP00000409200.1:p.Pro216Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.647C>A
  hgvsp: ENSP00000312697.5:p.Pro216Gln
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7435
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3553
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4512
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro216Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

1-44684368-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684368
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684368
    reference: chr 1
allele count: 1
allele frequency: 8.264326209484141e-6
allele num: 121002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3746G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.661G>A
  hgvsp: ENSP00000401099.1:p.Gly221Arg
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.661G>A
  hgvsp: ENSP00000409200.1:p.Gly221Arg
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.661G>A
  hgvsp: ENSP00000361363.2:p.Gly221Arg
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.661G>A
  hgvsp: ENSP00000354697.6:p.Gly221Arg
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.661G>A
  hgvsp: ENSP00000312697.5:p.Gly221Arg
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.739G>A
  hgvsp: ENSP00000402494.1:p.Gly247Arg
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.214G>A
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7406
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly221Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

1-44684373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684373
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684373
    reference: chr 1
allele count: 86
allele frequency: 7.125103562551781e-4
allele num: 120700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3751C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.666C>T
  hgvsp: ENST00000440641.1:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.666C>T
  hgvsp: ENST00000446292.1:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.219C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.744C>T
  hgvsp: ENST00000437511.1:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.666C>T
  hgvsp: ENST00000315913.5:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.666C>T
  hgvsp: ENST00000372289.2:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.666C>T
  hgvsp: ENST00000361745.6:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9117
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13113
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6602
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 15576
  bin: 9.75e1
  variant carriers: 86
genotype quality: GenotypeQuality
  all individuals: 4504
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18235
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His222His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

1-44684377-C-CGACG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684377
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684381
    reference: chr 1
allele count: 1
allele frequency: 8.291461452995706e-6
allele num: 120606
alternate allele: CGACG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.672_675dupACGG
  hgvsp: ENSP00000312697.5:p.Arg226ThrfsTer7
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.672_675dupACGG
  hgvsp: ENSP00000361363.2:p.Arg226ThrfsTer7
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.672_675dupACGG
  hgvsp: ENSP00000409200.1:p.Arg226ThrfsTer7
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3757_3760dupACGG
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.672_675dupACGG
  hgvsp: ENSP00000401099.1:p.Arg226ThrfsTer7
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.672_675dupACGG
  hgvsp: ENSP00000354697.6:p.Arg226ThrfsTer7
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.225_228dupACGG
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.750_753dupACGG
  hgvsp: ENSP00000402494.1:p.Arg252ThrfsTer7
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7357
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4962
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg226ThrfsTer7
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

1-44684377-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684377
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684377
    reference: chr 1
allele count: 1
allele frequency: 8.291461452995706e-6
allele num: 120606
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.670C>T
  hgvsp: ENSP00000361363.2:p.Arg224Ter
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.670C>T
  hgvsp: ENSP00000354697.6:p.Arg224Ter
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3755C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.670C>T
  hgvsp: ENSP00000401099.1:p.Arg224Ter
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.223C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.670C>T
  hgvsp: ENSP00000409200.1:p.Arg224Ter
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.748C>T
  hgvsp: ENSP00000402494.1:p.Arg250Ter
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.670C>T
  hgvsp: ENSP00000312697.5:p.Arg224Ter
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg224Ter
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

1-44684378-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684378
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684378
    reference: chr 1
allele count: 1
allele frequency: 8.299168423323983e-6
allele num: 120494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.224G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.749G>T
  hgvsp: ENSP00000402494.1:p.Arg250Leu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.671G>T
  hgvsp: ENSP00000409200.1:p.Arg224Leu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.671G>T
  hgvsp: ENSP00000361363.2:p.Arg224Leu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3756G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.671G>T
  hgvsp: ENSP00000312697.5:p.Arg224Leu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.671G>T
  hgvsp: ENSP00000401099.1:p.Arg224Leu
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.671G>T
  hgvsp: ENSP00000354697.6:p.Arg224Leu
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4509
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2144
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3548
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg224Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

1-44684381-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684381
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684381
    reference: chr 1
allele count: 3
allele frequency: 2.491528802072952e-5
allele num: 120408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.674G>A
  hgvsp: ENSP00000401099.1:p.Arg225Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.674G>A
  hgvsp: ENSP00000361363.2:p.Arg225Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.752G>A
  hgvsp: ENSP00000402494.1:p.Arg251Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.674G>A
  hgvsp: ENSP00000354697.6:p.Arg225Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.674G>A
  hgvsp: ENSP00000312697.5:p.Arg225Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.227G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.674G>A
  hgvsp: ENSP00000409200.1:p.Arg225Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3759G>A
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2143
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg225Gln
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum

1-44684383-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684383
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684383
    reference: chr 1
allele count: 1
allele frequency: 8.314625426124552e-6
allele num: 120270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.676C>T
  hgvsp: ENSP00000312697.5:p.Arg226Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.676C>T
  hgvsp: ENSP00000361363.2:p.Arg226Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.676C>T
  hgvsp: ENSP00000409200.1:p.Arg226Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.676C>T
  hgvsp: ENSP00000401099.1:p.Arg226Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.754C>T
  hgvsp: ENSP00000402494.1:p.Arg252Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.676C>T
  hgvsp: ENSP00000354697.6:p.Arg226Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.229C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3761C>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4509
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2143
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3546
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg226Trp
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

1-44684384-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684384
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684384
    reference: chr 1
allele count: 2
allele frequency: 1.664530519167069e-5
allele num: 120154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.755G>A
  hgvsp: ENSP00000402494.1:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.677G>A
  hgvsp: ENSP00000409200.1:p.Arg226Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.677G>A
  hgvsp: ENSP00000312697.5:p.Arg226Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3762G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.677G>A
  hgvsp: ENSP00000354697.6:p.Arg226Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.230G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.677G>A
  hgvsp: ENSP00000401099.1:p.Arg226Gln
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.677G>A
  hgvsp: ENSP00000361363.2:p.Arg226Gln
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4949
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4509
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg226Gln
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

1-44684402-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684402
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684402
    reference: chr 1
allele count: 1
allele frequency: 8.422896802668375e-6
allele num: 118724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.695G>A
  hgvsp: ENSP00000354697.6:p.Arg232His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.695G>A
  hgvsp: ENSP00000409200.1:p.Arg232His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3780G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.773G>A
  hgvsp: ENSP00000402494.1:p.Arg258His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.248G>A
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.695G>A
  hgvsp: ENSP00000312697.5:p.Arg232His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.695G>A
  hgvsp: ENSP00000401099.1:p.Arg232His
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.695G>A
  hgvsp: ENSP00000361363.2:p.Arg232His
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4942
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg232His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

1-44684411-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684411
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684411
    reference: chr 1
allele count: 1
allele frequency: 8.487523340689187e-6
allele num: 117820
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.704A>G
  hgvsp: ENSP00000361363.2:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.257A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.704A>G
  hgvsp: ENSP00000409200.1:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.704A>G
  hgvsp: ENSP00000312697.5:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3789A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.704A>G
  hgvsp: ENSP00000354697.6:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.782A>G
  hgvsp: ENSP00000402494.1:p.Asn261Ser
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.704A>G
  hgvsp: ENSP00000401099.1:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15257
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4936
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4497
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn235Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

1-44684413-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684413
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684413
    reference: chr 1
allele count: 12
allele frequency: 1.020442872206538e-4
allele num: 117596
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000401099
  ensembl transcript: ENST00000440641
  gene symbol: DMAP1
  hgvsc: ENST00000440641.1:c.706C>T
  hgvsp: ENSP00000401099.1:p.Arg236Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.706C>T
  hgvsp: ENSP00000312697.5:p.Arg236Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.259C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.706C>T
  hgvsp: ENSP00000354697.6:p.Arg236Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.706C>T
  hgvsp: ENSP00000409200.1:p.Arg236Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.784C>T
  hgvsp: ENSP00000402494.1:p.Arg262Trp
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3791C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.706C>T
  hgvsp: ENSP00000361363.2:p.Arg236Trp
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12207
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4496
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7101
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15218
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg236Trp
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum

1-44684430-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684430
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684430
    reference: chr 1
allele count: 2
allele frequency: 1.721259273284335e-5
allele num: 116194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.720+3A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.720+3A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.720+3A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.273+3A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3805+3A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.720+3A>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.798+3A>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4900
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15494
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 3.25e1
  variant carriers: 0
hgvs: c.720+3A>T
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-44684435-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684435
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684434
    reference: chr 1
allele count: 1
allele frequency: 8.646180981860312e-6
allele num: 115658
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3805+10delA
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.798+10delA
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.720+10delA
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.720+10delA
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.720+10delA
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.720+10delA
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.273+10delA
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3175
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15486
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4478
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: CA
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

1-44684438-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684438
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684438
    reference: chr 1
allele count: 1
allele frequency: 8.663859576163989e-6
allele num: 115422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3805+11G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.720+11G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.273+11G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.720+11G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.720+11G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.798+11G>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.720+11G>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6947
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3685
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/1-44684441-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684441
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684440
    reference: chr 1
allele count: 1
allele frequency: 8.688550228508871e-6
allele num: 115094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.720+15delA
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.720+15delA
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3805+15delA
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.720+15delA
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.798+15delA
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.720+15delA
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.273+15delA
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9069
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6927
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4468
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3543
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3645
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: CA
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

1-44684444-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684444
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684444
    reference: chr 1
allele count: 1
allele frequency: 8.706402688537151e-6
allele num: 114858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3805+17A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.720+17A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.720+17A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.798+17A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.720+17A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.720+17A>G
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.273+17A>G
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3646
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4467
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6891
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

1-44684463-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684463
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684463
    reference: chr 1
allele count: 4
allele frequency: 3.551325532254914e-5
allele num: 112634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.720+36C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.720+36C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.720+36C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3805+36C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.720+36C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.273+36C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.798+36C>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11948
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10302
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11949
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2884
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

1-44684474-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684474
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684474
    reference: chr 1
allele count: 1
allele frequency: 8.963464916998316e-6
allele num: 111564
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.798+47C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.720+47C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3805+47C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.720+47C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.720+47C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.720+47C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.273+47C>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2076
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1659
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1535
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2864
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4295
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

1-44684680-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684680
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684680
    reference: chr 1
allele count: 1
allele frequency: 8.561937052638789e-6
allele num: 116796
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.721-48T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.721-48T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.721-48T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.274-48T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.721-48T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3806-48T>C
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.799-48T>C
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26250
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11879
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2937
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32211
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

1-44684683-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44684683
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44684683
    reference: chr 1
allele count: 3
allele frequency: 2.572104667512603e-5
allele num: 116636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000409200
  ensembl transcript: ENST00000446292
  gene symbol: DMAP1
  hgvsc: ENST00000446292.1:c.721-45C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000483741
  gene symbol: DMAP1
  hgvsc: ENST00000483741.1:n.274-45C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000312697
  ensembl transcript: ENST00000315913
  gene symbol: DMAP1
  hgvsc: ENST00000315913.5:c.721-45C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000361363
  ensembl transcript: ENST00000372289
  gene symbol: DMAP1
  hgvsc: ENST00000372289.2:c.721-45C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000402494
  ensembl transcript: ENST00000437511
  gene symbol: DMAP1
  hgvsc: ENST00000437511.1:c.799-45C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl protein: ENSP00000354697
  ensembl transcript: ENST00000361745
  gene symbol: DMAP1
  hgvsc: ENST00000361745.6:c.721-45C>T
  variant of: http://identifiers.org/hgnc/18291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178028
  ensembl transcript: ENST00000488433
  gene symbol: DMAP1
  hgvsc: ENST00000488433.1:n.3806-45C>T
  variant of: http://identifiers.org/hgnc/18291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11859
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 2807
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1080
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40524
bin: 6.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1794
bin: 9.75e1
variant carriers: 3

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: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495190146543199e-5
allele num: 66738
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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.222e0

DP
type: SiteQuality
SIO_000300: 1.490455e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 1.36e1

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2412
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

GenotypeQuality
all individuals: 1055
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2807
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1080
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7522
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3508
bin: 7.75e1
variant carriers: 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: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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: 16512
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: 908
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.56e1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

DP
type: SiteQuality
SIO_000300: 1.490296e6

FS
type: SiteQuality
SIO_000300: 3.191e0

VQSLOD
type: SiteQuality
SIO_000300: 6.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.235e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

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

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

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

GenotypeQuality
all individuals: 1804
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 3508
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2807
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1080
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40517
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7522
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.155535012710885e-3
allele num: 8654
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: 66740
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.24e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

QD
type: SiteQuality
SIO_000300: 1.338e1

MQRankSum
type: SiteQuality
SIO_000300: 5.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

DP
type: SiteQuality
SIO_000300: 1.491566e6

GenotypeQuality
all individuals: 40515
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2807
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1804
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1080
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3508
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7522
bin: 6.75e1
variant carriers: 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: 66740
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 1.490907e6

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.05e1

FS
type: SiteQuality
SIO_000300: 2.377e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

GenotypeQuality
all individuals: 3508
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7522
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1080
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1804
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2807
bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 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: 8654
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.757e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.92e-1

MQ
type: SiteQuality
SIO_000300: 5.808e1

MQRankSum
type: SiteQuality
SIO_000300: -6.26e-1

FS
type: SiteQuality
SIO_000300: 5.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.53e-1

DP
type: SiteQuality
SIO_000300: 1.490906e6

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
all individuals: 7521
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3508
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2807
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40510
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
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: 1
allele frequency: 1.155535012710885e-4
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

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: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.56e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.718e0

VQSLOD
type: SiteQuality
SIO_000300: -1.411e0

QD
type: SiteQuality
SIO_000300: 7.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.490734e6

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1055
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3508
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7519
bin: 6.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e0

VQSLOD
type: SiteQuality
SIO_000300: 3.55e0

DP
type: SiteQuality
SIO_000300: 1.490725e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

QD
type: SiteQuality
SIO_000300: 1.111e1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

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

GenotypeQuality
all individuals: 40501
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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FS
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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East Asian
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South Asian
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Latino
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African
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European (Non-Finnish)
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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QD
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FS
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DP
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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Other
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African
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East Asian
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Latino
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VQSLOD
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DP
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QD
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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Latino
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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QD
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FS
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DP
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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allele num: 66720
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Other
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ClippingRankSum
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MQ
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FS
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ReadPosRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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allele frequency: 8.637070305752289e-5
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Other
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Other
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Latino
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European (Non-Finnish)
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European (Finnish)
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East Asian
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DP
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FS
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InbreedingCoeff
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MQ
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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East Asian
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South Asian
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Latino
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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MQ
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BaseQRankSum
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FS
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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Latino
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Other
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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QD
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InbreedingCoeff
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MQRankSum
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FS
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DP
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ClippingRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2791
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1056
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 16446
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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.59e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

FS
type: SiteQuality
SIO_000300: 4.778e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.963e0

MQRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.59e-2

QD
type: SiteQuality
SIO_000300: 1.282e1

DP
type: SiteQuality
SIO_000300: 1.485995e6

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 39060
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GenotypeQuality
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bin: 4.25e1
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: 16420
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: 2
allele frequency: 2.999850007499625e-5
allele num: 66670
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: 6614
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.481846e6

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

MQRankSum
type: SiteQuality
SIO_000300: 4.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.7e0

QD
type: SiteQuality
SIO_000300: 1.153e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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: 8654
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
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: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.389e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.64e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 7.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

DP
type: SiteQuality
SIO_000300: 1.475943e6

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

QD
type: SiteQuality
SIO_000300: 1.438e1

FS
type: SiteQuality
SIO_000300: 5.083e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 1080
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2405
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001741009785676e-5
allele num: 66628
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16350
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.731e0

VQSLOD
type: SiteQuality
SIO_000300: 4.55e-1

FS
type: SiteQuality
SIO_000300: 5.975e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.43e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

QD
type: SiteQuality
SIO_000300: 1.155e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-1

DP
type: SiteQuality
SIO_000300: 1.475789e6

GenotypeQuality
all individuals: 37728
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2774
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 9.25e1
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: 16350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500870504892838e-5
allele num: 66628
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.975e0

DP
type: SiteQuality
SIO_000300: 1.475789e6

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.731e0

VQSLOD
type: SiteQuality
SIO_000300: 4.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

QD
type: SiteQuality
SIO_000300: 1.155e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.43e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2405
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16244
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: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.476079e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

FS
type: SiteQuality
SIO_000300: 7.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

QD
type: SiteQuality
SIO_000300: 1.554e1

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.235e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 4
allele frequency: 2.5230225810521e-4
allele num: 15854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66444
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

FS
type: SiteQuality
SIO_000300: 6.611e0

DP
type: SiteQuality
SIO_000300: 2.207892e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

QD
type: SiteQuality
SIO_000300: 1.462e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQ
type: SiteQuality
SIO_000300: 6.004e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66428
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.327512022272843e-5
allele num: 15804
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: -2.042e-1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.206676e6

MQ
type: SiteQuality
SIO_000300: 5.932e1

QD
type: SiteQuality
SIO_000300: 9.16e0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15784
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66414
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
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African
type: Population
allele count: 3
allele frequency: 2.884060757546626e-4
allele num: 10402
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.77e-1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQ
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66404
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
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FS
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MQRankSum
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DP
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BaseQRankSum
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MQ
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.504981488727689e-5
allele num: 66446
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11570
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Other
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allele frequency: 0.0e0
allele num: 894
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
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VQSLOD
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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SIO_000300: 3.21e-1

FS
type: SiteQuality
SIO_000300: 9.97e-1

ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505343971097396e-5
allele num: 66430
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.872e1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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ClippingRankSum
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MQRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15864
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.009238361770636e-5
allele num: 66462
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.03e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.96e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15864
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504619180885318e-5
allele num: 66462
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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MQ
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QD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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DP
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.504438092372499e-5
allele num: 66470
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European (Finnish)
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ClippingRankSum
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MQ
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BaseQRankSum
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VQSLOD
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DP
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QD
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
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allele num: 66464
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Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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African
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Latino
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InbreedingCoeff
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ClippingRankSum
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MQ
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BaseQRankSum
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VQSLOD
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DP
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QD
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FS
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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Latino
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MQ
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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FS
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ClippingRankSum
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MQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

MQ
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SIO_000300: 5.961e1

ReadPosRankSum
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BaseQRankSum
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SIO_000300: 2.94e0

FS
type: SiteQuality
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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QD
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16178
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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QD
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ReadPosRankSum
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MQ
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MQRankSum
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BaseQRankSum
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SIO_000300: 2.94e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.004356316659156e-5
allele num: 66570
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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SIO_000300: -2.22e-1

MQ
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SIO_000300: 6.0e1

VQSLOD
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BaseQRankSum
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ReadPosRankSum
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QD
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50177209106746e-5
allele num: 66588
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16282
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

MQRankSum
type: SiteQuality
SIO_000300: 2.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.42e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.496e0

DP
type: SiteQuality
SIO_000300: 2.233506e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00336376741951e-5
allele num: 66592
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

QD
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SIO_000300: 1.583e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.007e0

DP
type: SiteQuality
SIO_000300: 2.233976e6

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

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

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: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66606
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.235093e6

BaseQRankSum
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002101471029721e-5
allele num: 66620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16338
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.56e0

MQ
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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QD
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VQSLOD
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InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 3.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.76e0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 5
allele frequency: 7.502776027130038e-5
allele num: 66642
num of homozygotes: 0

Other
type: Population
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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FS
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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allele frequency: 1.500510173458976e-5
allele num: 66644
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African
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allele frequency: 1.921968095329617e-4
allele num: 10406
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BaseQRankSum
type: SiteQuality
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DP
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ClippingRankSum
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MQ
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FS
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Latino
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African
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South Asian
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Other
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European (Finnish)
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MQ
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ClippingRankSum
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BaseQRankSum
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FS
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DP
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InbreedingCoeff
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VQSLOD
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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Latino
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Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66648
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MQ
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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VQSLOD
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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South Asian
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East Asian
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Latino
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European (Finnish)
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MQ
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
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QD
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DP
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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South Asian
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InbreedingCoeff
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QD
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MQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66664
num of homozygotes: 0

Latino
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East Asian
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Other
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South Asian
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African
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European (Finnish)
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MQRankSum
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MQ
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DP
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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Latino
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East Asian
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FS
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ClippingRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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QD
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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African
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Latino
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Other
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QD
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DP
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Latino
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QD
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MQ
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MQRankSum
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ReadPosRankSum
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DP
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BaseQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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Latino
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African
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VQSLOD
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DP
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504211793020457e-5
allele num: 66480
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
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

African
type: Population
allele count: 83
allele frequency: 7.980769230769231e-3
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16076
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.92e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

DP
type: SiteQuality
SIO_000300: 2.232549e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.284e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 4.58e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 43
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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: 10400
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16026
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.226183e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.99e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: -7.8e-2

FS
type: SiteQuality
SIO_000300: 5.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.417e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.167e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4509
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16026
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.8e-2

MQ
type: SiteQuality
SIO_000300: 5.957e1

DP
type: SiteQuality
SIO_000300: 2.226183e6

FS
type: SiteQuality
SIO_000300: 5.3e-1

QD
type: SiteQuality
SIO_000300: 1.417e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.167e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3276
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variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 904
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15946
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.055e0

DP
type: SiteQuality
SIO_000300: 2.224435e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.859e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.35e0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

QD
type: SiteQuality
SIO_000300: 1.459e1

GenotypeQuality
all individuals: 126
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4957
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
all individuals: 18029
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GenotypeQuality
all individuals: 3545
bin: 9.25e1
variant carriers: 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: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.518616700807326e-5
allele num: 66392
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 4.7e-1

MQ
type: SiteQuality
SIO_000300: 5.916e1

QD
type: SiteQuality
SIO_000300: 1.221e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.222e0

DP
type: SiteQuality
SIO_000300: 2.223034e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.06e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17880
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7311
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507068149621726e-5
allele num: 66354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15786
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.419e0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 2.22152e6

QD
type: SiteQuality
SIO_000300: 1.309e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.22e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 160
bin: 3.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15718
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507886245061673e-5
allele num: 66318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e0

VQSLOD
type: SiteQuality
SIO_000300: -8.129e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.569e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.219123e6

QD
type: SiteQuality
SIO_000300: 1.031e1

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517128379403465e-5
allele num: 65914
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.689e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 7.96e0

MQ
type: SiteQuality
SIO_000300: 5.852e1

VQSLOD
type: SiteQuality
SIO_000300: -1.172e0

DP
type: SiteQuality
SIO_000300: 2.195233e6

GenotypeQuality
all individuals: 2890
bin: 2.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14200
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523275651961979e-5
allele num: 65648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.180555e6

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.612e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
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InbreedingCoeff
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GenotypeQuality
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variant carriers: 11

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

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

East Asian
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allele frequency: 1.157943492357573e-4
allele num: 8636
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African
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allele frequency: 9.686168151879117e-5
allele num: 10324
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European (Non-Finnish)
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allele count: 10
allele frequency: 1.525041176111755e-4
allele num: 65572
num of homozygotes: 0

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

InbreedingCoeff
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MQ
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QD
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.068331748028597e-5
allele num: 65182
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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DP
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MQ
type: SiteQuality
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QD
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FS
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BaseQRankSum
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

South Asian
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allele frequency: 7.830853563038371e-5
allele num: 12770
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6590
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East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.991e1

FS
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SIO_000300: 4.077e0

QD
type: SiteQuality
SIO_000300: 1.32e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

DP
type: SiteQuality
SIO_000300: 2.154471e6

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.538698261270965e-5
allele num: 64990
num of homozygotes: 0

African
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: -6.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.465e0

FS
type: SiteQuality
SIO_000300: 1.5201e1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 2.151087e6

GenotypeQuality
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variant carriers: 0

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

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 8.063215610385422e-5
allele num: 12402
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64906
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East Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 3.85e-1

DP
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BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 1.871e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-2

FS
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MQ
type: SiteQuality
SIO_000300: 6.03e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 840
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64818
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Latino
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele num: 8604
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South Asian
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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ReadPosRankSum
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VQSLOD
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MQ
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MQRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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European (Finnish)
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African
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allele frequency: 2.94811320754717e-4
allele num: 10176
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ClippingRankSum
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MQ
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MQRankSum
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DP
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
type: SiteQuality
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10134
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East Asian
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South Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 64396
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Other
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East Asian
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African
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European (Finnish)
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South Asian
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FS
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QD
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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DP
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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