http://identifiers.org/exac.variant/7-151932859-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932859
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932859
    reference: chr 7
allele count: 1
allele frequency: 8.438818565400844e-6
allele num: 118500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+43G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+43G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+43G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+43G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+43G>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36829
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48628
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2601
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 938
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

7-151932861-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932861
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932861
    reference: chr 7
allele count: 2
allele frequency: 1.688675740484312e-5
allele num: 118436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+41C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+41C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+41C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+41C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+41C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36829
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1236
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2679
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

7-151932873-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932873
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932873
    reference: chr 7
allele count: 2
allele frequency: 1.688191103232886e-5
allele num: 118470
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+29T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+29T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+29T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+29T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+29T>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36830
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 528
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

7-151932874-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932874
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932874
    reference: chr 7
allele count: 2
allele frequency: 1.687564338390401e-5
allele num: 118514
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+28C>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+28C>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+28C>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+28C>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+28C>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36829
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2380
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48624
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

7-151932875-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932875
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932874
    reference: chr 7
allele count: 6
allele frequency: 5.063376597073368e-5
allele num: 118498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+26delC
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+26delC
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+26delC
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+26delC
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+26delC
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36830
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48599
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: AG
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

7-151932876-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932876
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932876
    reference: chr 7
allele count: 1990
allele frequency: 1.816820655151006e-2
allele num: 109532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+26C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+26C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+26C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+26C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+26C>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 9.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 5.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 1.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 2.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 3.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 6.75e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 8.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 2.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 7.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 37771
  bin: 9.75e1
  variant carriers: 1232
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 7.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 8.25e1
  variant carriers: 87
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 8.75e1
  variant carriers: 47
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 4.75e1
  variant carriers: 72
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 1.75e1
  variant carriers: 94
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 3.75e1
  variant carriers: 67
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 2.75e1
  variant carriers: 86
genotype quality: GenotypeQuality
  all individuals: 1043
  bin: 7.25e1
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 4.25e1
  variant carriers: 87
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 7.75e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 1939
  bin: 6.25e1
  variant carriers: 49
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 3.25e1
  variant carriers: 63
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 1.25e1
  variant carriers: 81
genotype quality: GenotypeQuality
  all individuals: 3454
  bin: 2.5e0
  variant carriers: 70
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 7.5e0
  variant carriers: 100
genotype quality: GenotypeQuality
  all individuals: 1169
  bin: 6.75e1
  variant carriers: 55
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 2.25e1
  variant carriers: 78
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

7-151932879-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932879
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932879
    reference: chr 7
allele count: 1
allele frequency: 8.410994852471151e-6
allele num: 118892
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+23T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+23T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+23T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+23T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+23T>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37130
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1205
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 833
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

7-151932881-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932881
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932881
    reference: chr 7
allele count: 2
allele frequency: 1.681944327642755e-5
allele num: 118910
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+21A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+21A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+21A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+21A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+21A>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37130
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2286
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1205
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-151932883-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932883
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932883
    reference: chr 7
allele count: 1
allele frequency: 8.408448809363649e-6
allele num: 118928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+19A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+19A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+19A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+19A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+19A>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37130
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

7-151932883-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932883
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932883
    reference: chr 7
allele count: 2
allele frequency: 1.68168976187273e-5
allele num: 118928
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+19A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+19A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+19A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+19A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+19A>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37130
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

7-151932886-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932886
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932886
    reference: chr 7
allele count: 1
allele frequency: 8.406893652795292e-6
allele num: 118950
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+16T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+16T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+16T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+16T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+16T>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37130
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/7-151932893-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932893
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932893
    reference: chr 7
allele count: 7
allele frequency: 5.876229810953293e-5
allele num: 119124
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+9T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+9T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+9T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+9T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+9T>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37131
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3506
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48255
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1014
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

7-151932895-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932895
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932895
    reference: chr 7
allele count: 3
allele frequency: 2.51724311534008e-5
allele num: 119178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+7C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+7C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+7C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+7C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+7C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37130
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3643
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1476
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 3.25e1
  variant carriers: 0
hgvs: c.2769+7C>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

7-151932896-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932896
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932896
    reference: chr 7
allele count: 1
allele frequency: 8.387150884844418e-6
allele num: 119230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+6G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+6G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+6G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+6G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+6G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37131
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1067
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3672
  bin: 6.25e1
  variant carriers: 0
hgvs: c.2769+6G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/7-151932897-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932897
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932897
    reference: chr 7
allele count: 15609
allele frequency: 1.45008453949202e-1
allele num: 107642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.480+5G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*289+5G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2769+5G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2769+5G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.235+5G>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.75e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 6.75e1
  variant carriers: 275
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.5e0
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 8.25e1
  variant carriers: 327
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 6.25e1
  variant carriers: 190
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 4.25e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 2.75e1
  variant carriers: 297
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 9.25e1
  variant carriers: 401
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.75e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 7.25e1
  variant carriers: 282
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 3.25e1
  variant carriers: 354
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 3.75e1
  variant carriers: 262
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 8.75e1
  variant carriers: 404
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.75e1
  variant carriers: 311
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 40200
  bin: 9.75e1
  variant carriers: 12760
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 2.25e1
  variant carriers: 219
genotype quality: GenotypeQuality
  all individuals: 1723
  bin: 2.25e1
  variant carriers: 375
genotype quality: GenotypeQuality
  all individuals: 3244
  bin: 2.5e0
  variant carriers: 276
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 5.25e1
  variant carriers: 351
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 1.75e1
  variant carriers: 326
genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 3.25e1
  variant carriers: 343
genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 3.75e1
  variant carriers: 323
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 2.75e1
  variant carriers: 337
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 8.25e1
  variant carriers: 277
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 7.75e1
  variant carriers: 278
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 279
genotype quality: GenotypeQuality
  all individuals: 35184
  bin: 9.75e1
  variant carriers: 11057
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 4.25e1
  variant carriers: 306
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 7.5e0
  variant carriers: 372
hgvs: c.2769+5G>T
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-151932907-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932907
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932907
    reference: chr 7
allele count: 2
allele frequency: 1.667778519012675e-5
allele num: 119920
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2764C>T
  hgvsp: ENSP00000262189.6:p.Pro922Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.230C>T
  hgvsp: ENSP00000403483.1:p.Pro78Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*284C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.475C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2764C>T
  hgvsp: ENSP00000347325.2:p.Pro922Ser
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39956
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50808
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro922Ser
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

7-151932908-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932908
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932908
    reference: chr 7
allele count: 56232
allele frequency: 4.79002334020478e-1
allele num: 117394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2763A>G
  hgvsp: ENST00000355193.2:c.2763A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.474A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2763A>G
  hgvsp: ENST00000262189.6:c.2763A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.229A>G
  hgvsp: ENST00000418673.1:c.229A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*283A>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 266
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.25e1
  variant carriers: 533
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 2.75e1
  variant carriers: 424
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 7.75e1
  variant carriers: 1113
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 3.75e1
  variant carriers: 521
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 8.25e1
  variant carriers: 1201
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 5.25e1
  variant carriers: 552
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 2.25e1
  variant carriers: 382
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.75e1
  variant carriers: 576
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 3.25e1
  variant carriers: 476
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.75e1
  variant carriers: 565
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.25e1
  variant carriers: 703
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.75e1
  variant carriers: 334
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 8.75e1
  variant carriers: 1269
genotype depth: GenotypeDepth
  all individuals: 44655
  bin: 9.75e1
  variant carriers: 44498
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.75e1
  variant carriers: 794
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 9.25e1
  variant carriers: 1381
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.25e1
  variant carriers: 915
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 6.75e1
  variant carriers: 118
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 1.25e1
  variant carriers: 72
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 8.25e1
  variant carriers: 117
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 4.75e1
  variant carriers: 115
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 7.5e0
  variant carriers: 84
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 7.75e1
  variant carriers: 103
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 2.25e1
  variant carriers: 93
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 3.75e1
  variant carriers: 115
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 1.75e1
  variant carriers: 80
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.75e1
  variant carriers: 86
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 2.5e0
  variant carriers: 57
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 3.25e1
  variant carriers: 97
genotype quality: GenotypeQuality
  all individuals: 55029
  bin: 9.75e1
  variant carriers: 54792
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 9.25e1
  variant carriers: 98
hgvs: p.Leu921Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

7-151932910-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932910
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932910
    reference: chr 7
allele count: 2
allele frequency: 1.658292290599141e-5
allele num: 120606
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.472T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.227T>C
  hgvsp: ENST00000418673.1:c.227T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2761T>C
  hgvsp: ENST00000262189.6:c.2761T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2761T>C
  hgvsp: ENST00000355193.2:c.2761T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*281T>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42831
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1141
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu921Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

7-151932912-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932912
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932912
    reference: chr 7
allele count: 7
allele frequency: 5.804311774461028e-5
allele num: 120600
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.470T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2759T>C
  hgvsp: ENSP00000347325.2:p.Val920Ala
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2759T>C
  hgvsp: ENSP00000262189.6:p.Val920Ala
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*279T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.225T>C
  hgvsp: ENSP00000403483.1:p.Val76Ala
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42830
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 54029
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val920Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-151932913-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932913
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932913
    reference: chr 7
allele count: 6
allele frequency: 4.977270464877061e-5
allele num: 120548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.469G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2758G>T
  hgvsp: ENSP00000347325.2:p.Val920Leu
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.224G>T
  hgvsp: ENSP00000403483.1:p.Val76Leu
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*278G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2758G>T
  hgvsp: ENSP00000262189.6:p.Val920Leu
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42829
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53994
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Val920Leu
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

7-151932914-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932914
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932914
    reference: chr 7
allele count: 1
allele frequency: 8.293386853323161e-6
allele num: 120578
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.468T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2757T>C
  hgvsp: ENST00000262189.6:c.2757T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.223T>C
  hgvsp: ENST00000418673.1:c.223T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2757T>C
  hgvsp: ENST00000355193.2:c.2757T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*277T>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42829
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54029
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val919Val
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

7-151932916-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932916
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932916
    reference: chr 7
allele count: 32362
allele frequency: 3.064119072867748e-1
allele num: 105616
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*275G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.466G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.221G>C
  hgvsp: ENSP00000403483.1:p.Val75Leu
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2755G>C
  hgvsp: ENSP00000262189.6:p.Val919Leu
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2755G>C
  hgvsp: ENSP00000347325.2:p.Val919Leu
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 4.25e1
  variant carriers: 401
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 8.75e1
  variant carriers: 830
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 2.75e1
  variant carriers: 255
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 3.75e1
  variant carriers: 363
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 7.25e1
  variant carriers: 606
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 8.25e1
  variant carriers: 772
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 6.25e1
  variant carriers: 471
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 9.25e1
  variant carriers: 890
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 399
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 5.25e1
  variant carriers: 410
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 297
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 5.75e1
  variant carriers: 424
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 7.75e1
  variant carriers: 689
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 2.25e1
  variant carriers: 208
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 6.75e1
  variant carriers: 557
genotype depth: GenotypeDepth
  all individuals: 43036
  bin: 9.75e1
  variant carriers: 26105
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 3.25e1
  variant carriers: 388
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 3.75e1
  variant carriers: 427
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 1.25e1
  variant carriers: 392
genotype quality: GenotypeQuality
  all individuals: 4640
  bin: 2.5e0
  variant carriers: 320
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 6.25e1
  variant carriers: 445
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 2.25e1
  variant carriers: 378
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 7.5e0
  variant carriers: 406
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 2.75e1
  variant carriers: 432
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 6.75e1
  variant carriers: 437
genotype quality: GenotypeQuality
  all individuals: 1017
  bin: 1.75e1
  variant carriers: 413
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 8.75e1
  variant carriers: 419
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 4.25e1
  variant carriers: 413
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 8.25e1
  variant carriers: 416
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 5.25e1
  variant carriers: 457
hgvs: p.Val919Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

7-151932918-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932918
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932918
    reference: chr 7
allele count: 3
allele frequency: 2.490246534406906e-5
allele num: 120470
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2753C>G
  hgvsp: ENSP00000262189.6:p.Ala918Gly
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.464C>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.219C>G
  hgvsp: ENSP00000403483.1:p.Ala74Gly
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*273C>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2753C>G
  hgvsp: ENSP00000347325.2:p.Ala918Gly
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37890
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1419
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1724
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala918Gly
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

7-151932921-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932921
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932921
    reference: chr 7
allele count: 2
allele frequency: 1.660164356271271e-5
allele num: 120470
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2750G>A
  hgvsp: ENSP00000262189.6:p.Gly917Glu
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2750G>A
  hgvsp: ENSP00000347325.2:p.Gly917Glu
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.216G>A
  hgvsp: ENSP00000403483.1:p.Gly73Glu
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.461G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*270G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37886
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1421
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50067
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly917Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

7-151932922-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932922
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932922
    reference: chr 7
allele count: 13
allele frequency: 1.07925017018945e-4
allele num: 120454
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.460G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.215G>A
  hgvsp: ENSP00000403483.1:p.Gly73Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*269G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2749G>A
  hgvsp: ENSP00000262189.6:p.Gly917Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2749G>A
  hgvsp: ENSP00000347325.2:p.Gly917Arg
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37886
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50066
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly917Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum

7-151932923-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932923
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932923
    reference: chr 7
allele count: 12071
allele frequency: 1.2028179680338e-1
allele num: 100356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*268C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.459C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2748C>T
  hgvsp: ENST00000355193.2:c.2748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.214C>T
  hgvsp: ENST00000418673.1:c.214C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2748C>T
  hgvsp: ENST00000262189.6:c.2748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 2.75e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 7.25e1
  variant carriers: 443
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 8.25e1
  variant carriers: 525
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 351
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 2.25e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 3.75e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 8.75e1
  variant carriers: 525
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.25e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.25e1
  variant carriers: 329
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.25e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 4.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 7.75e1
  variant carriers: 463
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 9.25e1
  variant carriers: 609
genotype depth: GenotypeDepth
  all individuals: 37856
  bin: 9.75e1
  variant carriers: 9822
genotype quality: GenotypeQuality
  all individuals: 1932
  bin: 2.25e1
  variant carriers: 530
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 7.5e0
  variant carriers: 595
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 6.25e1
  variant carriers: 420
genotype quality: GenotypeQuality
  all individuals: 1984
  bin: 7.75e1
  variant carriers: 372
genotype quality: GenotypeQuality
  all individuals: 2190
  bin: 6.75e1
  variant carriers: 402
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 1.25e1
  variant carriers: 557
genotype quality: GenotypeQuality
  all individuals: 2022
  bin: 7.25e1
  variant carriers: 392
genotype quality: GenotypeQuality
  all individuals: 1543
  bin: 3.75e1
  variant carriers: 481
genotype quality: GenotypeQuality
  all individuals: 1522
  bin: 5.25e1
  variant carriers: 455
genotype quality: GenotypeQuality
  all individuals: 1521
  bin: 1.75e1
  variant carriers: 544
genotype quality: GenotypeQuality
  all individuals: 5643
  bin: 2.5e0
  variant carriers: 423
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 3.25e1
  variant carriers: 486
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 2.75e1
  variant carriers: 490
genotype quality: GenotypeQuality
  all individuals: 1996
  bin: 8.25e1
  variant carriers: 349
hgvs: p.Ile916Ile
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/7-151932927-CCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932927
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932925
    reference: chr 7
allele count: 1
allele frequency: 8.315455104857889e-6
allele num: 120258
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2742_2743delTG
  hgvsp: ENSP00000347325.2:p.Ser914ArgfsTer19
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*262_*263delTG
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.453_454delTG
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2742_2743delTG
  hgvsp: ENSP00000262189.6:p.Ser914ArgfsTer19
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.208_209delTG
  hgvsp: ENSP00000403483.1:p.Ser70ArgfsTer19
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27735
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2376
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1675
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1674
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser914ArgfsTer19
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: CCA
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

7-151932945-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932945
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932945
    reference: chr 7
allele count: 9730
allele frequency: 9.618996777191213e-2
allele num: 101154
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2726G>A
  hgvsp: ENSP00000262189.6:p.Arg909Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.437G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2726G>A
  hgvsp: ENSP00000347325.2:p.Arg909Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.192G>A
  hgvsp: ENSP00000403483.1:p.Arg65Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*246G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 4.75e1
  variant carriers: 258
genotype depth: GenotypeDepth
  all individuals: 28314
  bin: 9.75e1
  variant carriers: 5968
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 3.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 2.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 5.75e1
  variant carriers: 375
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 8.25e1
  variant carriers: 540
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 5.25e1
  variant carriers: 326
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 2.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 7.25e1
  variant carriers: 520
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 6.25e1
  variant carriers: 460
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 7.75e1
  variant carriers: 562
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 4.25e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 3.75e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 6.75e1
  variant carriers: 500
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 9.25e1
  variant carriers: 538
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 8.75e1
  variant carriers: 561
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 1.25e1
  variant carriers: 366
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 3.75e1
  variant carriers: 300
genotype quality: GenotypeQuality
  all individuals: 2063
  bin: 6.75e1
  variant carriers: 241
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 8.25e1
  variant carriers: 209
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 3.25e1
  variant carriers: 327
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 2.75e1
  variant carriers: 305
genotype quality: GenotypeQuality
  all individuals: 5970
  bin: 2.5e0
  variant carriers: 316
genotype quality: GenotypeQuality
  all individuals: 1776
  bin: 8.75e1
  variant carriers: 216
genotype quality: GenotypeQuality
  all individuals: 26551
  bin: 9.75e1
  variant carriers: 5748
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 4.25e1
  variant carriers: 300
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 1.75e1
  variant carriers: 367
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 5.25e1
  variant carriers: 289
genotype quality: GenotypeQuality
  all individuals: 1647
  bin: 2.25e1
  variant carriers: 376
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 7.5e0
  variant carriers: 391
hgvs: p.Arg909Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

7-151932946-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932946
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932946
    reference: chr 7
allele count: 1340
allele frequency: 1.147496060834418e-2
allele num: 116776
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*245A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.436A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2725A>G
  hgvsp: ENSP00000262189.6:p.Arg909Gly
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2725A>G
  hgvsp: ENSP00000347325.2:p.Arg909Gly
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.191A>G
  hgvsp: ENSP00000403483.1:p.Arg65Gly
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 9.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 7.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 5.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 7.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 8.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 6.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 4.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 4.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 8.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 5.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 22862
  bin: 9.75e1
  variant carriers: 915
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 6.25e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 3.25e1
  variant carriers: 74
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 4.75e1
  variant carriers: 63
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 4.25e1
  variant carriers: 64
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 7.25e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 5.75e1
  variant carriers: 60
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 7.5e0
  variant carriers: 80
genotype quality: GenotypeQuality
  all individuals: 1936
  bin: 6.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 42152
  bin: 9.75e1
  variant carriers: 584
genotype quality: GenotypeQuality
  all individuals: 1755
  bin: 8.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 1806
  bin: 9.25e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 2.5e0
  variant carriers: 70
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 1.25e1
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 1.75e1
  variant carriers: 77
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 8.25e1
  variant carriers: 31
hgvs: p.Arg909Gly
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: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

7-151932948-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932948
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932948
    reference: chr 7
allele count: 2
allele frequency: 1.68177460856696e-5
allele num: 118922
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2723G>A
  hgvsp: ENSP00000347325.2:p.Gly908Asp
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.189G>A
  hgvsp: ENSP00000403483.1:p.Gly64Asp
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2723G>A
  hgvsp: ENSP00000262189.6:p.Gly908Asp
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.434G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*243G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21322
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1666
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46022
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1868
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 1
hgvs: p.Gly908Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/7-151932949-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932949
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932949
    reference: chr 7
allele count: 345
allele frequency: 2.918041106318194e-3
allele num: 118230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*242G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2722G>T
  hgvsp: ENSP00000347325.2:p.Gly908Cys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.433G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2722G>T
  hgvsp: ENSP00000262189.6:p.Gly908Cys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.188G>T
  hgvsp: ENSP00000403483.1:p.Gly64Cys
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 7.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 8.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4016
  bin: 8.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 21322
  bin: 9.75e1
  variant carriers: 218
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 3.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 2.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 7.5e0
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 1.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1884
  bin: 6.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.5e0
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 1769
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 1.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 1667
  bin: 8.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 9.25e1
  variant carriers: 8
hgvs: p.Gly908Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

7-151932950-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932950
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932950
    reference: chr 7
allele count: 1
allele frequency: 8.406045628015669e-6
allele num: 118962
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.187A>C
  hgvsp: ENST00000418673.1:c.187A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2721A>C
  hgvsp: ENST00000262189.6:c.2721A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2721A>C
  hgvsp: ENST00000355193.2:c.2721A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*241A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.432A>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20951
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1749
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1868
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg907Arg
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

7-151932953-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932953
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932953
    reference: chr 7
allele count: 3
allele frequency: 2.522577064729327e-5
allele num: 118926
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2718C>T
  hgvsp: ENST00000262189.6:c.2718C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*238C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.429C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2718C>T
  hgvsp: ENST00000355193.2:c.2718C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.184C>T
  hgvsp: ENST00000418673.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20941
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1756
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1866
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly906Gly
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

7-151932955-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932955
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932955
    reference: chr 7
allele count: 3
allele frequency: 2.527422534499318e-5
allele num: 118698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*236G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2716G>A
  hgvsp: ENSP00000347325.2:p.Gly906Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2716G>A
  hgvsp: ENSP00000262189.6:p.Gly906Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.427G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.182G>A
  hgvsp: ENSP00000403483.1:p.Gly62Ser
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20929
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1750
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1954
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1675
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly906Ser
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-151932960-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932960
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932960
    reference: chr 7
allele count: 1
allele frequency: 8.429997302400863e-6
allele num: 118624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.177G>A
  hgvsp: ENSP00000403483.1:p.Arg60Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*231G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2711G>A
  hgvsp: ENSP00000347325.2:p.Arg904Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.422G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2711G>A
  hgvsp: ENSP00000262189.6:p.Arg904Gln
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20924
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1774
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1645
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46019
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1749
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg904Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum

7-151932961-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932961
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932961
    reference: chr 7
allele count: 4517
allele frequency: 4.240438594844258e-2
allele num: 106522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2710C>T
  hgvsp: ENSP00000347325.2:p.Arg904Ter
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*230C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.176C>T
  hgvsp: ENSP00000403483.1:p.Arg60Ter
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.421C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2710C>T
  hgvsp: ENSP00000262189.6:p.Arg904Ter
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 5.75e1
  variant carriers: 379
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 5.25e1
  variant carriers: 261
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 7.25e1
  variant carriers: 445
genotype depth: GenotypeDepth
  all individuals: 19313
  bin: 9.75e1
  variant carriers: 1854
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 2.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 7.75e1
  variant carriers: 469
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 7.5e0
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 3.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 8.25e1
  variant carriers: 462
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 6.25e1
  variant carriers: 400
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 9.25e1
  variant carriers: 423
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 8.75e1
  variant carriers: 429
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 4.75e1
  variant carriers: 238
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 6.75e1
  variant carriers: 445
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 4.25e1
  variant carriers: 139
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 4.75e1
  variant carriers: 246
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 1.25e1
  variant carriers: 430
genotype quality: GenotypeQuality
  all individuals: 2849
  bin: 2.5e0
  variant carriers: 390
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 3.25e1
  variant carriers: 306
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 5.25e1
  variant carriers: 212
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 2.75e1
  variant carriers: 343
genotype quality: GenotypeQuality
  all individuals: 2192
  bin: 7.75e1
  variant carriers: 138
genotype quality: GenotypeQuality
  all individuals: 2155
  bin: 9.25e1
  variant carriers: 127
genotype quality: GenotypeQuality
  all individuals: 2061
  bin: 8.75e1
  variant carriers: 113
genotype quality: GenotypeQuality
  all individuals: 1531
  bin: 5.75e1
  variant carriers: 215
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 3.75e1
  variant carriers: 305
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 2.25e1
  variant carriers: 354
genotype quality: GenotypeQuality
  all individuals: 1367
  bin: 1.75e1
  variant carriers: 410
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 235
hgvs: p.Arg904Ter
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

7-151932961-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932961
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932961
    reference: chr 7
allele count: 1
allele frequency: 9.387732111676462e-6
allele num: 106522
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2710C>A
  hgvsp: ENST00000262189.6:c.2710C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2710C>A
  hgvsp: ENST00000355193.2:c.2710C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.176C>A
  hgvsp: ENST00000418673.1:c.176C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*230C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.421C>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19313
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26535
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2849
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1531
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1637
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2461
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2155
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2192
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1367
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2173
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg904Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

7-151932962-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932962
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932962
    reference: chr 7
allele count: 3
allele frequency: 2.533527007397899e-5
allele num: 118412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.420G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2709G>A
  hgvsp: ENST00000262189.6:c.2709G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2709G>A
  hgvsp: ENST00000355193.2:c.2709G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*229G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.175G>A
  hgvsp: ENST00000418673.1:c.175G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4130
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3744
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17684
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1662
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1455
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly903Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

http://identifiers.org/exac.variant/7-151932965-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932965
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932965
    reference: chr 7
allele count: 3
allele frequency: 3.009510051763573e-5
allele num: 99684
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2706G>T
  hgvsp: ENST00000262189.6:c.2706G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2706G>T
  hgvsp: ENST00000355193.2:c.2706G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.417G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.172G>T
  hgvsp: ENST00000418673.1:c.172G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*226G>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 18180
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4363
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1883
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1510
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5643
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1566
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1267
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1780
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1379
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser902Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

7-151932965-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932965
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932965
    reference: chr 7
allele count: 32011
allele frequency: 3.211247542233458e-1
allele num: 99684
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2706G>A
  hgvsp: ENST00000262189.6:c.2706G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.172G>A
  hgvsp: ENST00000418673.1:c.172G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*226G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.417G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2706G>A
  hgvsp: ENST00000355193.2:c.2706G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 4.75e1
  variant carriers: 925
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 2.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.25e1
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.5e0
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.25e1
  variant carriers: 525
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 6.75e1
  variant carriers: 2283
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 6.25e1
  variant carriers: 1969
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 9.25e1
  variant carriers: 2453
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 8.75e1
  variant carriers: 2590
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 5.25e1
  variant carriers: 1191
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 7.75e1
  variant carriers: 2646
genotype depth: GenotypeDepth
  all individuals: 18180
  bin: 9.75e1
  variant carriers: 12013
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 2.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 8.25e1
  variant carriers: 2630
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 5.75e1
  variant carriers: 1548
genotype depth: GenotypeDepth
  all individuals: 4363
  bin: 7.25e1
  variant carriers: 2565
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.75e1
  variant carriers: 350
genotype quality: GenotypeQuality
  all individuals: 1883
  bin: 7.5e0
  variant carriers: 593
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 610
genotype quality: GenotypeQuality
  all individuals: 28698
  bin: 9.75e1
  variant carriers: 23363
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 3.75e1
  variant carriers: 605
genotype quality: GenotypeQuality
  all individuals: 1267
  bin: 5.25e1
  variant carriers: 578
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 9.25e1
  variant carriers: 505
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 5.75e1
  variant carriers: 562
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 3.25e1
  variant carriers: 602
genotype quality: GenotypeQuality
  all individuals: 1566
  bin: 1.75e1
  variant carriers: 629
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 2.25e1
  variant carriers: 627
genotype quality: GenotypeQuality
  all individuals: 1780
  bin: 6.25e1
  variant carriers: 623
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 7.25e1
  variant carriers: 564
genotype quality: GenotypeQuality
  all individuals: 5643
  bin: 2.5e0
  variant carriers: 450
genotype quality: GenotypeQuality
  all individuals: 1510
  bin: 1.25e1
  variant carriers: 571
hgvs: p.Ser902Ser
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

7-151932966-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932966
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932966
    reference: chr 7
allele count: 2
allele frequency: 1.691045911896508e-5
allele num: 118270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*225C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2705C>T
  hgvsp: ENSP00000262189.6:p.Ser902Leu
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.171C>T
  hgvsp: ENSP00000403483.1:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2705C>T
  hgvsp: ENSP00000347325.2:p.Ser902Leu
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.416C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4820
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40565
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2133
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3341
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2765
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser902Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/7-151932968-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932968
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932968
    reference: chr 7
allele count: 1
allele frequency: 8.45522955948254e-6
allele num: 118270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.414G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*223G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2703G>T
  hgvsp: ENST00000262189.6:c.2703G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2703G>T
  hgvsp: ENST00000355193.2:c.2703G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.169G>T
  hgvsp: ENST00000418673.1:c.169G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4722
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2557
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2489
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2132
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2349
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2764
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu901Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

7-151932969-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932969
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932969
    reference: chr 7
allele count: 88
allele frequency: 7.440602012344635e-4
allele num: 118270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2702T>C
  hgvsp: ENSP00000347325.2:p.Leu901Pro
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.413T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*222T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.168T>C
  hgvsp: ENSP00000403483.1:p.Leu57Pro
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2702T>C
  hgvsp: ENSP00000262189.6:p.Leu901Pro
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5485
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4716
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2759
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3354
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2486
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40582
  bin: 9.75e1
  variant carriers: 88
hgvs: p.Leu901Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

7-151932975-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932975
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932975
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 118170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2696C>T
  hgvsp: ENSP00000347325.2:p.Ala899Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*216C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.162C>T
  hgvsp: ENSP00000403483.1:p.Ala55Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.407C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2696C>T
  hgvsp: ENSP00000262189.6:p.Ala899Val
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2557
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 1
hgvs: p.Ala899Val
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

7-151932980-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932980
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932980
    reference: chr 7
allele count: 1
allele frequency: 8.461382251404589e-6
allele num: 118184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2691A>T
  hgvsp: ENST00000355193.2:c.2691A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.402A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2691A>T
  hgvsp: ENST00000262189.6:c.2691A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.157A>T
  hgvsp: ENST00000418673.1:c.157A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*211A>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5786
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4818
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2485
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3305
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2383
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2344
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg897Arg
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

7-151932982-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932982
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932982
    reference: chr 7
allele count: 1381
allele frequency: 1.215604809605127e-2
allele num: 113606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.400C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.155C>T
  hgvsp: ENSP00000403483.1:p.Arg53Ter
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2689C>T
  hgvsp: ENSP00000262189.6:p.Arg897Ter
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2689C>T
  hgvsp: ENSP00000347325.2:p.Arg897Ter
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*209C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 5.25e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 8.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 2.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 3.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 5.75e1
  variant carriers: 201
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 6.75e1
  variant carriers: 195
genotype depth: GenotypeDepth
  all individuals: 4835
  bin: 4.75e1
  variant carriers: 161
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 9.75e1
  variant carriers: 165
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 3.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 4661
  bin: 7.25e1
  variant carriers: 166
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 4.25e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 6.25e1
  variant carriers: 223
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 8.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 9.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 110
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 4.25e1
  variant carriers: 70
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 3.25e1
  variant carriers: 96
genotype quality: GenotypeQuality
  all individuals: 1187
  bin: 2.25e1
  variant carriers: 97
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 5.75e1
  variant carriers: 63
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 2.75e1
  variant carriers: 97
genotype quality: GenotypeQuality
  all individuals: 2491
  bin: 7.25e1
  variant carriers: 49
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 3.75e1
  variant carriers: 98
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 1.75e1
  variant carriers: 137
genotype quality: GenotypeQuality
  all individuals: 1007
  bin: 7.5e0
  variant carriers: 138
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 2.5e0
  variant carriers: 112
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 5.25e1
  variant carriers: 68
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 1.25e1
  variant carriers: 137
genotype quality: GenotypeQuality
  all individuals: 2841
  bin: 6.75e1
  variant carriers: 64
genotype quality: GenotypeQuality
  all individuals: 2625
  bin: 9.25e1
  variant carriers: 41
hgvs: p.Arg897Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

7-151932982-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932982
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932982
    reference: chr 7
allele count: 1
allele frequency: 8.802351988451315e-6
allele num: 113606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.155C>A
  hgvsp: ENST00000418673.1:c.155C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2689C>A
  hgvsp: ENST00000355193.2:c.2689C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*209C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.400C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2689C>A
  hgvsp: ENST00000262189.6:c.2689C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4835
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1007
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2841
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33002
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2625
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg897Arg
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

7-151932985-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932985
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932985
    reference: chr 7
allele count: 17
allele frequency: 1.441264243081932e-4
allele num: 117952
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2686C>T
  hgvsp: ENSP00000262189.6:p.Pro896Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.397C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2686C>T
  hgvsp: ENSP00000347325.2:p.Pro896Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*206C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.152C>T
  hgvsp: ENSP00000403483.1:p.Pro52Ser
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6145
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3494
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2893
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2679
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2530
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro896Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

7-151932987-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932987
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932987
    reference: chr 7
allele count: 2
allele frequency: 1.690817171939198e-5
allele num: 118286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.150G>A
  hgvsp: ENSP00000403483.1:p.Arg51Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*204G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.395G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2684G>A
  hgvsp: ENSP00000262189.6:p.Arg895Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2684G>A
  hgvsp: ENSP00000347325.2:p.Arg895Lys
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2560
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2336
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2750
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2594
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg895Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

7-151932990-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932990
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932990
    reference: chr 7
allele count: 1059
allele frequency: 9.881312283059008e-3
allele num: 107172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*201G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2681G>A
  hgvsp: ENSP00000347325.2:p.Arg894Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.147G>A
  hgvsp: ENSP00000403483.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2681G>A
  hgvsp: ENSP00000262189.6:p.Arg894Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.392G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 9.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 8.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 4.25e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 6202
  bin: 5.75e1
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 3.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 9.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 8.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 3.75e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 5.25e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 7.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 2.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 4.75e1
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 5381
  bin: 6.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 2.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 7.25e1
  variant carriers: 79
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 2.75e1
  variant carriers: 83
genotype quality: GenotypeQuality
  all individuals: 1043
  bin: 5.75e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 833
  bin: 3.75e1
  variant carriers: 61
genotype quality: GenotypeQuality
  all individuals: 2272
  bin: 8.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 983
  bin: 4.75e1
  variant carriers: 65
genotype quality: GenotypeQuality
  all individuals: 2546
  bin: 9.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 2.25e1
  variant carriers: 96
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 1.25e1
  variant carriers: 127
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 3.25e1
  variant carriers: 76
genotype quality: GenotypeQuality
  all individuals: 3575
  bin: 6.25e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 27322
  bin: 9.75e1
  variant carriers: 276
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 7.5e0
  variant carriers: 131
genotype quality: GenotypeQuality
  all individuals: 3794
  bin: 2.5e0
  variant carriers: 89
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 1.75e1
  variant carriers: 105
hgvs: p.Arg894Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

7-151932991-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932991
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932991
    reference: chr 7
allele count: 1908
allele frequency: 1.690500239221732e-2
allele num: 112866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*200C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2680C>T
  hgvsp: ENSP00000262189.6:p.Arg894Trp
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.391C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.146C>T
  hgvsp: ENSP00000403483.1:p.Arg50Trp
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2680C>T
  hgvsp: ENSP00000347325.2:p.Arg894Trp
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 8.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 2.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 8.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 3.75e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 4.75e1
  variant carriers: 305
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 3.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 5.75e1
  variant carriers: 293
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 7.75e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 6.25e1
  variant carriers: 289
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 9.75e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 7.25e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 5.25e1
  variant carriers: 339
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 9.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 4.25e1
  variant carriers: 253
genotype quality: GenotypeQuality
  all individuals: 2553
  bin: 9.25e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 7.5e0
  variant carriers: 215
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 3.75e1
  variant carriers: 121
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 1.25e1
  variant carriers: 161
genotype quality: GenotypeQuality
  all individuals: 4416
  bin: 6.25e1
  variant carriers: 71
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 5.75e1
  variant carriers: 90
genotype quality: GenotypeQuality
  all individuals: 1423
  bin: 2.25e1
  variant carriers: 153
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 2.75e1
  variant carriers: 133
genotype quality: GenotypeQuality
  all individuals: 2636
  bin: 7.25e1
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 4.25e1
  variant carriers: 131
genotype quality: GenotypeQuality
  all individuals: 29518
  bin: 9.75e1
  variant carriers: 498
genotype quality: GenotypeQuality
  all individuals: 1216
  bin: 2.5e0
  variant carriers: 146
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 1.75e1
  variant carriers: 165
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 3.25e1
  variant carriers: 124
hgvs: p.Arg894Trp
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum

7-151932993-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932993
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932993
    reference: chr 7
allele count: 1
allele frequency: 8.448229251148959e-6
allele num: 118368
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2678A>T
  hgvsp: ENSP00000262189.6:p.Lys893Met
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2678A>T
  hgvsp: ENSP00000347325.2:p.Lys893Met
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*198A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.389A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.144A>T
  hgvsp: ENSP00000403483.1:p.Lys49Met
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4972
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2530
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2896
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4235
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys893Met
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

7-151932996-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932996
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932996
    reference: chr 7
allele count: 43
allele frequency: 3.632247601027166e-4
allele num: 118384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*195G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2675G>A
  hgvsp: ENSP00000262189.6:p.Gly892Glu
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.141G>A
  hgvsp: ENSP00000403483.1:p.Gly48Glu
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.386G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2675G>A
  hgvsp: ENSP00000347325.2:p.Gly892Glu
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5357
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4151
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39562
  bin: 9.75e1
  variant carriers: 44
hgvs: p.Gly892Glu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

7-151932997-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151932997
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151932997
    reference: chr 7
allele count: 26659
allele frequency: 2.692882684498677e-1
allele num: 98998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*194G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.140G>A
  hgvsp: ENSP00000403483.1:p.Gly48Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.385G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2674G>A
  hgvsp: ENSP00000347325.2:p.Gly892Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2674G>A
  hgvsp: ENSP00000262189.6:p.Gly892Arg
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 5.25e1
  variant carriers: 3118
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 2.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 3.25e1
  variant carriers: 599
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 7.25e1
  variant carriers: 2566
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 2.75e1
  variant carriers: 266
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 3.75e1
  variant carriers: 1085
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 6.25e1
  variant carriers: 3356
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 7.75e1
  variant carriers: 1944
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 4.25e1
  variant carriers: 1869
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 6.75e1
  variant carriers: 2998
genotype depth: GenotypeDepth
  all individuals: 5979
  bin: 5.75e1
  variant carriers: 3388
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 4.75e1
  variant carriers: 2509
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 9.75e1
  variant carriers: 2308
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 8.25e1
  variant carriers: 1417
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 9.25e1
  variant carriers: 746
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 8.75e1
  variant carriers: 1088
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 1.25e1
  variant carriers: 757
genotype quality: GenotypeQuality
  all individuals: 1792
  bin: 2.75e1
  variant carriers: 733
genotype quality: GenotypeQuality
  all individuals: 3932
  bin: 6.25e1
  variant carriers: 613
genotype quality: GenotypeQuality
  all individuals: 1837
  bin: 7.25e1
  variant carriers: 622
genotype quality: GenotypeQuality
  all individuals: 1644
  bin: 5.25e1
  variant carriers: 682
genotype quality: GenotypeQuality
  all individuals: 21088
  bin: 9.75e1
  variant carriers: 16743
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 8.25e1
  variant carriers: 567
genotype quality: GenotypeQuality
  all individuals: 1776
  bin: 4.25e1
  variant carriers: 713
genotype quality: GenotypeQuality
  all individuals: 1735
  bin: 3.75e1
  variant carriers: 673
genotype quality: GenotypeQuality
  all individuals: 4880
  bin: 2.5e0
  variant carriers: 591
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 4.75e1
  variant carriers: 684
genotype quality: GenotypeQuality
  all individuals: 2504
  bin: 2.25e1
  variant carriers: 730
genotype quality: GenotypeQuality
  all individuals: 2080
  bin: 7.5e0
  variant carriers: 678
genotype quality: GenotypeQuality
  all individuals: 2440
  bin: 6.75e1
  variant carriers: 725
hgvs: p.Gly892Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

7-151933009-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933009
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933009
    reference: chr 7
allele count: 28
allele frequency: 2.364625206904706e-4
allele num: 118412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2662T>A
  hgvsp: ENSP00000347325.2:p.Ser888Thr
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.373T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2662T>A
  hgvsp: ENSP00000262189.6:p.Ser888Thr
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.128T>A
  hgvsp: ENSP00000403483.1:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*182T>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10077
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6682
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3970
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26175
  bin: 9.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9873
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5081
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser888Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP

7-151933014-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933014
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933014
    reference: chr 7
allele count: 86
allele frequency: 7.3713443274934e-4
allele num: 116668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.123G>A
  hgvsp: ENSP00000403483.1:p.Arg42His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*177G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2657G>A
  hgvsp: ENSP00000262189.6:p.Arg886His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2657G>A
  hgvsp: ENSP00000347325.2:p.Arg886His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.368G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8528
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 5.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10065
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8793
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6679
  bin: 4.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 2.5e0
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 3810
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 4.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 7.5e0
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 2.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2674
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9591
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3946
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 3.75e1
  variant carriers: 4
hgvs: p.Arg886His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

7-151933021-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933021
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933021
    reference: chr 7
allele count: 9
allele frequency: 7.607905459094829e-5
allele num: 118298
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-3T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-3T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-3T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-3T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-3T>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8987
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8512
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10000
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9256
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4034
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2703
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4249
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.75e1
  variant carriers: 0
hgvs: c.2653-3T>C
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

7-151933028-AGATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933028
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933024
    reference: chr 7
allele count: 1
allele frequency: 8.468404383246109e-6
allele num: 118086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-14_2653-11delAATC
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-14_*173-11delAATC
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-14_364-11delAATC
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-14_119-11delAATC
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-14_2653-11delAATC
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2670
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8112
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1595
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4245
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4035
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: AGATT
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

7-151933030-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933030
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933029
    reference: chr 7
allele count: 1
allele frequency: 8.468260957929679e-6
allele num: 118088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-13delA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-13delA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-13delA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-13delA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-13delA
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8471
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1675
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4166
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4036
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25244
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2662
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8063
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: AT
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

7-151933032-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933032
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933032
    reference: chr 7
allele count: 1
allele frequency: 8.471991595784337e-6
allele num: 118036
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-14A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-14A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-14A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-14A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-14A>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7672
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4037
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2657
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4168
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4674
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2347
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25243
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

7-151933033-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933033
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933033
    reference: chr 7
allele count: 15199
allele frequency: 1.745005740528129e-1
allele num: 87100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-15C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-15C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-15C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-15C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-15C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.75e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 7.25e1
  variant carriers: 279
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 4.75e1
  variant carriers: 2227
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 2.25e1
  variant carriers: 714
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8427
  bin: 4.25e1
  variant carriers: 2923
genotype depth: GenotypeDepth
  all individuals: 9027
  bin: 3.75e1
  variant carriers: 2860
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 3.25e1
  variant carriers: 2591
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.75e1
  variant carriers: 202
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.75e1
  variant carriers: 404
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 1.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 2.75e1
  variant carriers: 1667
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.25e1
  variant carriers: 157
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 5.25e1
  variant carriers: 1593
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 6.25e1
  variant carriers: 657
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 9.75e1
  variant carriers: 747
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 5.75e1
  variant carriers: 1063
genotype quality: GenotypeQuality
  all individuals: 2344
  bin: 4.75e1
  variant carriers: 701
genotype quality: GenotypeQuality
  all individuals: 2704
  bin: 1.25e1
  variant carriers: 852
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 5.75e1
  variant carriers: 586
genotype quality: GenotypeQuality
  all individuals: 3175
  bin: 7.5e0
  variant carriers: 898
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 5.25e1
  variant carriers: 561
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 8.75e1
  variant carriers: 413
genotype quality: GenotypeQuality
  all individuals: 2628
  bin: 3.75e1
  variant carriers: 748
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 9.25e1
  variant carriers: 392
genotype quality: GenotypeQuality
  all individuals: 4005
  bin: 2.25e1
  variant carriers: 854
genotype quality: GenotypeQuality
  all individuals: 7786
  bin: 2.5e0
  variant carriers: 687
genotype quality: GenotypeQuality
  all individuals: 2799
  bin: 2.75e1
  variant carriers: 786
genotype quality: GenotypeQuality
  all individuals: 2499
  bin: 6.75e1
  variant carriers: 499
genotype quality: GenotypeQuality
  all individuals: 9197
  bin: 9.75e1
  variant carriers: 6362
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 7.25e1
  variant carriers: 495
genotype quality: GenotypeQuality
  all individuals: 2742
  bin: 1.75e1
  variant carriers: 859
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

7-151933033-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933033
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933033
    reference: chr 7
allele count: 1
allele frequency: 1.148105625717566e-5
allele num: 87100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-15C>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-15C>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-15C>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-15C>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-15C>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3175
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2704
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2742
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7786
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2799
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2647
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2628
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9197
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

7-151933034-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933034
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933034
    reference: chr 7
allele count: 4
allele frequency: 3.39881721161036e-5
allele num: 117688
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-16C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-16C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-16C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-16C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-16C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15098
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3562
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9158
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3848
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7578
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

7-151933035-GAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933035
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933033
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 117682
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-19_119-18delTT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-19_*173-18delTT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-19_2653-18delTT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-19_2653-18delTT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-19_364-18delTT
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2437
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4778
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3547
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3835
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2238
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: GAA
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

7-151933042-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933042
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933042
    reference: chr 7
allele count: 1
allele frequency: 8.525730655117144e-6
allele num: 117292
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-24G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-24G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-24G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-24G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-24G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1241
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4655
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1267
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19312
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2227
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7572
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1569
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

7-151933053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933053
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933053
    reference: chr 7
allele count: 586
allele frequency: 6.189399860580072e-3
allele num: 94678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-35C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-35C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-35C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-35C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-35C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6753
  bin: 3.75e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 2.25e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 11488
  bin: 3.25e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11682
  bin: 2.75e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 4.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7032
  bin: 1.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 4.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 8.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 9.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 4572
  bin: 9.75e1
  variant carriers: 145
genotype quality: GenotypeQuality
  all individuals: 1857
  bin: 1.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 3415
  bin: 3.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 3387
  bin: 2.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 1982
  bin: 7.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 3951
  bin: 3.25e1
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 3794
  bin: 6.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 6317
  bin: 2.5e0
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 2139
  bin: 7.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 1802
  bin: 1.25e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 2317
  bin: 5.25e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 2795
  bin: 4.75e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 4842
  bin: 2.25e1
  variant carriers: 44
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

7-151933053-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933053
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933053
    reference: chr 7
allele count: 3830
allele frequency: 4.045290352563426e-2
allele num: 94678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-35C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-35C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-35C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-35C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-35C>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 1.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 6753
  bin: 3.75e1
  variant carriers: 670
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 11488
  bin: 3.25e1
  variant carriers: 1014
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 7032
  bin: 1.75e1
  variant carriers: 196
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 11682
  bin: 2.75e1
  variant carriers: 1063
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 4.25e1
  variant carriers: 430
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 2.25e1
  variant carriers: 648
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 4.75e1
  variant carriers: 231
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 9.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 3415
  bin: 3.75e1
  variant carriers: 254
genotype quality: GenotypeQuality
  all individuals: 4842
  bin: 2.25e1
  variant carriers: 233
genotype quality: GenotypeQuality
  all individuals: 4572
  bin: 9.75e1
  variant carriers: 1167
genotype quality: GenotypeQuality
  all individuals: 3951
  bin: 3.25e1
  variant carriers: 254
genotype quality: GenotypeQuality
  all individuals: 1802
  bin: 1.25e1
  variant carriers: 174
genotype quality: GenotypeQuality
  all individuals: 2646
  bin: 7.5e0
  variant carriers: 250
genotype quality: GenotypeQuality
  all individuals: 2139
  bin: 7.75e1
  variant carriers: 164
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 9.25e1
  variant carriers: 105
genotype quality: GenotypeQuality
  all individuals: 2795
  bin: 4.75e1
  variant carriers: 243
genotype quality: GenotypeQuality
  all individuals: 7062
  bin: 6.25e1
  variant carriers: 164
genotype quality: GenotypeQuality
  all individuals: 1982
  bin: 7.25e1
  variant carriers: 122
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 4.25e1
  variant carriers: 189
genotype quality: GenotypeQuality
  all individuals: 3387
  bin: 2.75e1
  variant carriers: 159
genotype quality: GenotypeQuality
  all individuals: 6317
  bin: 2.5e0
  variant carriers: 206
genotype quality: GenotypeQuality
  all individuals: 1857
  bin: 1.75e1
  variant carriers: 226
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

7-151933054-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933054
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933054
    reference: chr 7
allele count: 690
allele frequency: 6.282550897767418e-3
allele num: 109828
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-36T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-36T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-36T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-36T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-36T>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12234
  bin: 2.75e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 6124
  bin: 3.75e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 8347
  bin: 2.25e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 1.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 9.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 11062
  bin: 3.25e1
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 4.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 4.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2457
  bin: 4.25e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 3750
  bin: 3.25e1
  variant carriers: 58
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 1.75e1
  variant carriers: 55
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 7.5e0
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 2806
  bin: 5.25e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 1.25e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 5475
  bin: 6.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 4230
  bin: 2.25e1
  variant carriers: 60
genotype quality: GenotypeQuality
  all individuals: 5071
  bin: 9.75e1
  variant carriers: 169
genotype quality: GenotypeQuality
  all individuals: 9067
  bin: 6.25e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 2720
  bin: 7.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 2984
  bin: 2.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 8.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 1205
  bin: 8.75e1
  variant carriers: 21
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-151933058-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933058
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933058
    reference: chr 7
allele count: 10504
allele frequency: 1.698796739552335e-1
allele num: 61832
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-40T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-40T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-40T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-40T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-40T>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.75e1
  variant carriers: 564
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 361
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9592
  bin: 2.25e1
  variant carriers: 1792
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 4.25e1
  variant carriers: 978
genotype depth: GenotypeDepth
  all individuals: 9521
  bin: 1.75e1
  variant carriers: 811
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 1.25e1
  variant carriers: 184
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 9.75e1
  variant carriers: 564
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 3.75e1
  variant carriers: 1465
genotype depth: GenotypeDepth
  all individuals: 9476
  bin: 3.25e1
  variant carriers: 2091
genotype depth: GenotypeDepth
  all individuals: 12478
  bin: 2.75e1
  variant carriers: 2381
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.75e1
  variant carriers: 217
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 148
genotype quality: GenotypeQuality
  all individuals: 1644
  bin: 4.75e1
  variant carriers: 427
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 7.25e1
  variant carriers: 266
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 8.75e1
  variant carriers: 256
genotype quality: GenotypeQuality
  all individuals: 2519
  bin: 2.75e1
  variant carriers: 316
genotype quality: GenotypeQuality
  all individuals: 21181
  bin: 2.5e0
  variant carriers: 262
genotype quality: GenotypeQuality
  all individuals: 2380
  bin: 1.75e1
  variant carriers: 390
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 5.25e1
  variant carriers: 372
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 5.75e1
  variant carriers: 324
genotype quality: GenotypeQuality
  all individuals: 3233
  bin: 7.5e0
  variant carriers: 403
genotype quality: GenotypeQuality
  all individuals: 2479
  bin: 6.25e1
  variant carriers: 345
genotype quality: GenotypeQuality
  all individuals: 2623
  bin: 3.75e1
  variant carriers: 425
genotype quality: GenotypeQuality
  all individuals: 2280
  bin: 1.25e1
  variant carriers: 305
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 7.75e1
  variant carriers: 295
genotype quality: GenotypeQuality
  all individuals: 7121
  bin: 9.75e1
  variant carriers: 5478
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 8.25e1
  variant carriers: 268
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/7-151933060-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933060
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933061
    reference: chr 7
allele count: 3
allele frequency: 2.622056741307882e-5
allele num: 114414
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-43dupT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-43dupT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-43dupT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-43dupT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-43dupT
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7037
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16712
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2634
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2508
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5003
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5391
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5173
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

7-151933060-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933060
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933060
    reference: chr 7
allele count: 1
allele frequency: 8.74018913769294e-6
allele num: 114414
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-42G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-42G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-42G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-42G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-42G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7037
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2508
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5391
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3820
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5173
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4530
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5003
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1737
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

7-151933064-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933064
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933064
    reference: chr 7
allele count: 18
allele frequency: 1.576983056193163e-4
allele num: 114142
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-46T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-46T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-46T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-46T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-46T>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6912
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12573
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11529
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1710
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2662
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3063
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4613
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4223
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11863
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3087
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

7-151933064-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151933064
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151933064
    reference: chr 7
allele count: 1
allele frequency: 8.761016978850905e-6
allele num: 114142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-46T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2653-46T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2653-46T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.364-46T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*173-46T>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12573
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6912
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4223
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5125
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5419
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4613
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2662
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3831
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3087
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/7-151935755-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151935755
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151935755
    reference: chr 7
allele count: 33
allele frequency: 2.831985994541991e-4
allele num: 116526
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.2652+37T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*172+37T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000403483
  ensembl transcript: ENST00000418673
  gene symbol: KMT2C
  hgvsc: ENST00000418673.1:c.119-2737T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.363+37T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.2652+37T>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6760
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6429
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 1.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6350
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 2.5e0
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2918
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 162
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 6.75e1
variant carriers: 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: 896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9328
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: 1
allele frequency: 6.117704637220115e-5
allele num: 16346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65092
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.088e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 2.628e0

VQSLOD
type: SiteQuality
SIO_000300: -2.735e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
SIO_000300: 6.657734e6

MQ
type: SiteQuality
SIO_000300: 4.063e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

GenotypeQuality
all individuals: 48627
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 913
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 940
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.074747102050856e-5
allele num: 65046
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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.42e0

DP
type: SiteQuality
SIO_000300: 6.656808e6

MQ
type: SiteQuality
SIO_000300: 3.997e1

FS
type: SiteQuality
SIO_000300: 6.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.534e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

QD
type: SiteQuality
SIO_000300: 1.35e0

VQSLOD
type: SiteQuality
SIO_000300: -2.529e0

GenotypeQuality
all individuals: 1190
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2408
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 9.25e1
variant carriers: 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: 65080
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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: 1
allele frequency: 6.119951040391677e-5
allele num: 16340
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.072961373390558e-4
allele num: 9320
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

MQ
type: SiteQuality
SIO_000300: 3.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.39e-1

QD
type: SiteQuality
SIO_000300: 2.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: -3.526e0

FS
type: SiteQuality
SIO_000300: 4.505e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.32e-1

DP
type: SiteQuality
SIO_000300: 6.655816e6

VQSLOD
type: SiteQuality
SIO_000300: -4.181e0

GenotypeQuality
all individuals: 899
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 7.5e0
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65080
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: 9346
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.222792858889704e-4
allele num: 16356
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.662e0

DP
type: SiteQuality
SIO_000300: 6.655758e6

MQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

QD
type: SiteQuality
SIO_000300: 3.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.689e0

MQ
type: SiteQuality
SIO_000300: 4.104e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

GenotypeQuality
all individuals: 860
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2330
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65082
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.359056806002144e-4
allele num: 9330
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16356
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: 894
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.556e0

DP
type: SiteQuality
SIO_000300: 6.655959e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

FS
type: SiteQuality
SIO_000300: 3.003e0

VQSLOD
type: SiteQuality
SIO_000300: -5.799e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.283e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.21e-1

MQ
type: SiteQuality
SIO_000300: 4.164e1

QD
type: SiteQuality
SIO_000300: 9.3e-1

GenotypeQuality
all individuals: 1023
bin: 9.25e1
variant carriers: 42

GenotypeQuality
all individuals: 707
bin: 5.75e1
variant carriers: 63

GenotypeQuality
all individuals: 769
bin: 5.25e1
variant carriers: 61

GenotypeQuality
all individuals: 1026
bin: 8.25e1
variant carriers: 43

GenotypeQuality
all individuals: 40022
bin: 9.75e1
variant carriers: 1089

Other
type: Population
allele count: 17
allele frequency: 2.073170731707317e-2
allele num: 820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1479
allele frequency: 2.473161432728002e-2
allele num: 59802
num of homozygotes: 0

African
type: Population
allele count: 127
allele frequency: 1.430502365397612e-2
allele num: 8878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 75
allele frequency: 1.275510204081633e-2
allele num: 5880
num of homozygotes: 0

Latino
type: Population
allele count: 92
allele frequency: 8.505917159763314e-3
allele num: 10816
num of homozygotes: 0

South Asian
type: Population
allele count: 120
allele frequency: 8.012820512820512e-3
allele num: 14976
num of homozygotes: 0

East Asian
type: Population
allele count: 80
allele frequency: 9.569377990430622e-3
allele num: 8360
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.360000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.072e0

VQSLOD
type: SiteQuality
SIO_000300: -2.59e0

FS
type: SiteQuality
SIO_000300: 1.672e0

MQ
type: SiteQuality
SIO_000300: 4.25e1

QD
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.429e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.93e-2

DP
type: SiteQuality
SIO_000300: 6.762572e6

GenotypeQuality
all individuals: 48249
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 614
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1938
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9488
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 16326
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: 65342
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

FS
type: SiteQuality
SIO_000300: 1.472e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQ
type: SiteQuality
SIO_000300: 4.037e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.28e0

DP
type: SiteQuality
SIO_000300: 6.668183e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.559e0

VQSLOD
type: SiteQuality
SIO_000300: -4.496e0

QD
type: SiteQuality
SIO_000300: 3.27e0

GenotypeQuality
all individuals: 604
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48248
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9494
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.53031555106663e-5
allele num: 65346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 4.022e1

FS
type: SiteQuality
SIO_000300: 4.765e0

QD
type: SiteQuality
SIO_000300: 5.24e0

VQSLOD
type: SiteQuality
SIO_000300: -5.756e0

DP
type: SiteQuality
SIO_000300: 6.668804e6

MQRankSum
type: SiteQuality
SIO_000300: 5.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

GenotypeQuality
all individuals: 834
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48248
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 940
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529847321237341e-5
allele num: 65366
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9492
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

QD
type: SiteQuality
SIO_000300: 4.9e0

VQSLOD
type: SiteQuality
SIO_000300: -3.617e0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQ
type: SiteQuality
SIO_000300: 4.14e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

FS
type: SiteQuality
SIO_000300: 9.464e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

DP
type: SiteQuality
SIO_000300: 6.669416e6

GenotypeQuality
all individuals: 940
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48248
bin: 9.75e1
variant carriers: 2

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529847321237341e-5
allele num: 65366
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.617e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

QD
type: SiteQuality
SIO_000300: 4.9e0

FS
type: SiteQuality
SIO_000300: 9.464e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

MQ
type: SiteQuality
SIO_000300: 4.14e1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e0

DP
type: SiteQuality
SIO_000300: 6.669416e6

GenotypeQuality
all individuals: 990
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48248
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.052188552188552e-4
allele num: 9504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16336
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65370
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.97e0

DP
type: SiteQuality
SIO_000300: 6.671319e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.686e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

FS
type: SiteQuality
SIO_000300: 1.4647e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.49e-1

QD
type: SiteQuality
SIO_000300: 1.0e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.857e0

MQ
type: SiteQuality
SIO_000300: 3.911e1

GenotypeQuality
all individuals: 901
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 3.25e1
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: 3
allele frequency: 3.471418653089562e-4
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9570
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.582671391910057e-5
allele num: 65464
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.113216774666829e-5
allele num: 16358
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.648e0

QD
type: SiteQuality
SIO_000300: 6.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.54e0

FS
type: SiteQuality
SIO_000300: 1.2356e1

MQ
type: SiteQuality
SIO_000300: 4.152e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.22e-1

DP
type: SiteQuality
SIO_000300: 6.678948e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e0

GenotypeQuality
all individuals: 988
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48259
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 285
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 902
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.581411685654073e-5
allele num: 65482
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: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.8698e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.136e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

QD
type: SiteQuality
SIO_000300: 1.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.79e-1

DP
type: SiteQuality
SIO_000300: 6.680697e6

MQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

MQ
type: SiteQuality
SIO_000300: 4.046e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.103e0

VQSLOD
type: SiteQuality
SIO_000300: -4.651e0

GenotypeQuality
all individuals: 1068
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48271
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 858
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65538
num of homozygotes: 0

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

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

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: 11576
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.041666666666667e-4
allele num: 9600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.382e0

FS
type: SiteQuality
SIO_000300: 2.539e1

QD
type: SiteQuality
SIO_000300: 4.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.083e0

MQRankSum
type: SiteQuality
SIO_000300: -4.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

DP
type: SiteQuality
SIO_000300: 6.682945e6

MQ
type: SiteQuality
SIO_000300: 4.418e1

GenotypeQuality
all individuals: 1114
bin: 9.25e1
variant carriers: 236

GenotypeQuality
all individuals: 955
bin: 1.25e1
variant carriers: 329

GenotypeQuality
all individuals: 1423
bin: 6.75e1
variant carriers: 292

GenotypeQuality
all individuals: 1015
bin: 5.75e1
variant carriers: 311

GenotypeQuality
all individuals: 1199
bin: 8.75e1
variant carriers: 259

GenotypeQuality
all individuals: 2580
bin: 6.25e1
variant carriers: 284

GenotypeQuality
all individuals: 1010
bin: 4.75e1
variant carriers: 322

South Asian
type: Population
allele count: 1346
allele frequency: 9.267419443679427e-2
allele num: 14524
num of homozygotes: 0

Other
type: Population
allele count: 118
allele frequency: 1.428571428571428e-1
allele num: 826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 741
allele frequency: 1.227227558794303e-1
allele num: 6038
num of homozygotes: 0

African
type: Population
allele count: 1514
allele frequency: 1.771589047507606e-1
allele num: 8546
num of homozygotes: 0

East Asian
type: Population
allele count: 711
allele frequency: 8.788627935723115e-2
allele num: 8090
num of homozygotes: 0

Latino
type: Population
allele count: 1090
allele frequency: 1.045062320230105e-1
allele num: 10430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10089
allele frequency: 1.70456849361357e-1
allele num: 59188
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

DP
type: SiteQuality
SIO_000300: 7.307664e6

VQSLOD
type: SiteQuality
SIO_000300: 7.35e0

MQRankSum
type: SiteQuality
SIO_000300: -4.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-1

FS
type: SiteQuality
SIO_000300: 1.5347e1

MQ
type: SiteQuality
SIO_000300: 4.027e1

QD
type: SiteQuality
SIO_000300: 1.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.733e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.857e-1

GenotypeQuality
all individuals: 866
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 1012
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variant carriers: 1

GenotypeQuality
all individuals: 2575
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9828
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 16456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.035454103933948e-5
allele num: 65888
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.081e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

QD
type: SiteQuality
SIO_000300: 4.5e-1

DP
type: SiteQuality
SIO_000300: 7.264143e6

MQRankSum
type: SiteQuality
SIO_000300: -2.974e0

FS
type: SiteQuality
SIO_000300: 1.4418e1

VQSLOD
type: SiteQuality
SIO_000300: -4.737e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.72e-1

MQ
type: SiteQuality
SIO_000300: 4.179e1

GenotypeQuality
all individuals: 524
bin: 6.25e1
variant carriers: 108

GenotypeQuality
all individuals: 240
bin: 5.25e1
variant carriers: 117

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 86

GenotypeQuality
all individuals: 243
bin: 7.25e1
variant carriers: 109

GenotypeQuality
all individuals: 237
bin: 2.75e1
variant carriers: 82

GenotypeQuality
all individuals: 204
bin: 4.25e1
variant carriers: 92

African
type: Population
allele count: 4846
allele frequency: 4.929806714140387e-1
allele num: 9830
num of homozygotes: 0

South Asian
type: Population
allele count: 5927
allele frequency: 4.045733788395904e-1
allele num: 14650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3300
allele frequency: 4.993946731234867e-1
allele num: 6608
num of homozygotes: 0

Other
type: Population
allele count: 411
allele frequency: 4.670454545454545e-1
allele num: 880
num of homozygotes: 0

East Asian
type: Population
allele count: 4237
allele frequency: 4.959035580524345e-1
allele num: 8544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 31771
allele frequency: 4.862858542259773e-1
allele num: 65334
num of homozygotes: 0

Latino
type: Population
allele count: 5740
allele frequency: 4.970557672324212e-1
allele num: 11548
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.45e-1

MQ
type: SiteQuality
SIO_000300: 4.098e1

MQRankSum
type: SiteQuality
SIO_000300: -8.852e0

VQSLOD
type: SiteQuality
SIO_000300: 1.958e2

QD
type: SiteQuality
SIO_000300: 7.93e0

FS
type: SiteQuality
SIO_000300: 1.17542e2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.945e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.75e0

DP
type: SiteQuality
SIO_000300: 8.245856e6

GenotypeQuality
all individuals: 54027
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 711
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 109
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variant carriers: 1

GenotypeQuality
all individuals: 109
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
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: 11578
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: 0
allele frequency: 0.0e0
allele num: 66296
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: 2
allele frequency: 1.985702938840349e-4
allele num: 10072
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.116e1

QD
type: SiteQuality
SIO_000300: 2.7e-1

FS
type: SiteQuality
SIO_000300: 1.2769e1

DP
type: SiteQuality
SIO_000300: 7.81044e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.479e0

VQSLOD
type: SiteQuality
SIO_000300: -4.019e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.174e0

MQRankSum
type: SiteQuality
SIO_000300: -7.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.73e-1

GenotypeQuality
all individuals: 669
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
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variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.25e1
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: 0
allele frequency: 0.0e0
allele num: 66298
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.956867421983701e-4
allele num: 10062
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: 16488
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

VQSLOD
type: SiteQuality
SIO_000300: -4.999e0

FS
type: SiteQuality
SIO_000300: 1.9702e1

QD
type: SiteQuality
SIO_000300: 4.77e0

MQ
type: SiteQuality
SIO_000300: 4.023e1

DP
type: SiteQuality
SIO_000300: 7.810519e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.82e-1

GenotypeQuality
all individuals: 337
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
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variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
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variant carriers: 1

GenotypeQuality
all individuals: 516
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GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 1

African
type: Population
allele count: 3
allele frequency: 2.989238740534077e-4
allele num: 10036
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 3
allele frequency: 4.526115687516973e-5
allele num: 66282
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: 908
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e0

FS
type: SiteQuality
SIO_000300: 3.7458e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.413e0

VQSLOD
type: SiteQuality
SIO_000300: -9.73e0

MQRankSum
type: SiteQuality
SIO_000300: -2.972e0

QD
type: SiteQuality
SIO_000300: 6.3e-1

DP
type: SiteQuality
SIO_000300: 7.810585e6

MQ
type: SiteQuality
SIO_000300: 4.141e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

GenotypeQuality
all individuals: 708
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
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variant carriers: 0

GenotypeQuality
all individuals: 519
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GenotypeQuality
all individuals: 672
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variant carriers: 0

GenotypeQuality
all individuals: 38
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GenotypeQuality
all individuals: 805
bin: 6.75e1
variant carriers: 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: 10060
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508750754375377e-5
allele num: 66280
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: -4.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.099e0

FS
type: SiteQuality
SIO_000300: 3.6643e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.568e0

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

MQ
type: SiteQuality
SIO_000300: 3.843e1

DP
type: SiteQuality
SIO_000300: 7.810467e6

QD
type: SiteQuality
SIO_000300: 2.28e0

GenotypeQuality
all individuals: 1150
bin: 4.75e1
variant carriers: 457

GenotypeQuality
all individuals: 1203
bin: 7.75e1
variant carriers: 424

GenotypeQuality
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variant carriers: 26058

GenotypeQuality
all individuals: 1070
bin: 5.75e1
variant carriers: 432

GenotypeQuality
all individuals: 1176
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variant carriers: 409

GenotypeQuality
all individuals: 1116
bin: 9.25e1
variant carriers: 405

South Asian
type: Population
allele count: 4316
allele frequency: 2.986851211072664e-1
allele num: 14450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15302
allele frequency: 2.662235985942448e-1
allele num: 57478
num of homozygotes: 0

East Asian
type: Population
allele count: 2909
allele frequency: 3.769111168696553e-1
allele num: 7718
num of homozygotes: 0

African
type: Population
allele count: 3531
allele frequency: 3.892195767195767e-1
allele num: 9072
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2130
allele frequency: 3.613844587716322e-1
allele num: 5894
num of homozygotes: 0

Latino
type: Population
allele count: 3932
allele frequency: 3.85414624583415e-1
allele num: 10202
num of homozygotes: 0

Other
type: Population
allele count: 242
allele frequency: 3.017456359102245e-1
allele num: 802
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.079e-1

QD
type: SiteQuality
SIO_000300: 2.15e0

FS
type: SiteQuality
SIO_000300: 5.7453e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.428e1

MQ
type: SiteQuality
SIO_000300: 4.046e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.596e0

DP
type: SiteQuality
SIO_000300: 7.836793e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 74
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 50067
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variant carriers: 3

GenotypeQuality
all individuals: 142
bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.52980612429788e-5
allele num: 66228
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: -7.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.685e0

MQ
type: SiteQuality
SIO_000300: 4.06e1

QD
type: SiteQuality
SIO_000300: 6.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.512e0

FS
type: SiteQuality
SIO_000300: 2.201e0

DP
type: SiteQuality
SIO_000300: 6.958527e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.36e0

GenotypeQuality
all individuals: 1076
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1670
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GenotypeQuality
all individuals: 1252
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GenotypeQuality
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GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.020144362900547e-5
allele num: 66222
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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10006
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.339e0

MQRankSum
type: SiteQuality
SIO_000300: 3.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 6.958053e6

FS
type: SiteQuality
SIO_000300: 1.094e0

QD
type: SiteQuality
SIO_000300: 4.32e0

VQSLOD
type: SiteQuality
SIO_000300: -3.202e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.38e-1

MQ
type: SiteQuality
SIO_000300: 4.141e1

GenotypeQuality
all individuals: 160
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GenotypeQuality
all individuals: 98
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GenotypeQuality
all individuals: 1251
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GenotypeQuality
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GenotypeQuality
all individuals: 1246
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 6.75e1
variant carriers: 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: 16494
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: 11
allele frequency: 1.66143064282262e-4
allele num: 66208
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.998800719568259e-4
allele num: 10006
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: 8648
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-2

FS
type: SiteQuality
SIO_000300: 2.0488e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.24e0

MQ
type: SiteQuality
SIO_000300: 3.997e1

VQSLOD
type: SiteQuality
SIO_000300: -5.154e0

QD
type: SiteQuality
SIO_000300: 4.95e0

DP
type: SiteQuality
SIO_000300: 6.957957e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

GenotypeQuality
all individuals: 1909
bin: 9.25e1
variant carriers: 319

GenotypeQuality
all individuals: 23428
bin: 9.75e1
variant carriers: 5744

GenotypeQuality
all individuals: 1866
bin: 8.75e1
variant carriers: 307

GenotypeQuality
all individuals: 1507
bin: 4.25e1
variant carriers: 477

GenotypeQuality
all individuals: 1536
bin: 4.75e1
variant carriers: 482

GenotypeQuality
all individuals: 1464
bin: 5.75e1
variant carriers: 379

Other
type: Population
allele count: 85
allele frequency: 1.0625e-1
allele num: 800
num of homozygotes: 0

African
type: Population
allele count: 840
allele frequency: 1.031941031941032e-1
allele num: 8140
num of homozygotes: 0

South Asian
type: Population
allele count: 1240
allele frequency: 8.25346112886049e-2
allele num: 15024
num of homozygotes: 0

Latino
type: Population
allele count: 1294
allele frequency: 1.445810055865922e-1
allele num: 8950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 916
allele frequency: 1.670313639679066e-1
allele num: 5484
num of homozygotes: 0

East Asian
type: Population
allele count: 1167
allele frequency: 1.664764621968616e-1
allele num: 7010
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6529
allele frequency: 1.188214311712892e-1
allele num: 54948
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.452e0

FS
type: SiteQuality
SIO_000300: 3.7049e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.79e-1

DP
type: SiteQuality
SIO_000300: 6.931937e6

MQRankSum
type: SiteQuality
SIO_000300: -4.391e0

QD
type: SiteQuality
SIO_000300: 7.6e-1

MQ
type: SiteQuality
SIO_000300: 4.018e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.599e-1

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46477
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1749
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 9918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512767759893501e-5
allele num: 66104
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.103e0

QD
type: SiteQuality
SIO_000300: 2.11e0

DP
type: SiteQuality
SIO_000300: 5.672605e6

MQRankSum
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.112e0

MQ
type: SiteQuality
SIO_000300: 4.804e1

FS
type: SiteQuality
SIO_000300: 1.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.82e-1

GenotypeQuality
all individuals: 1220
bin: 5.75e1
variant carriers: 220

GenotypeQuality
all individuals: 1946
bin: 7.25e1
variant carriers: 219

GenotypeQuality
all individuals: 1788
bin: 9.25e1
variant carriers: 184

GenotypeQuality
all individuals: 2202
bin: 6.25e1
variant carriers: 257

GenotypeQuality
all individuals: 1274
bin: 4.75e1
variant carriers: 312

GenotypeQuality
all individuals: 1917
bin: 7.75e1
variant carriers: 249

European (Finnish)
type: Population
allele count: 696
allele frequency: 1.286031042128603e-1
allele num: 5412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6397
allele frequency: 1.161064324088863e-1
allele num: 55096
num of homozygotes: 0

African
type: Population
allele count: 428
allele frequency: 4.85921889191644e-2
allele num: 8808
num of homozygotes: 0

East Asian
type: Population
allele count: 399
allele frequency: 5.25e-2
allele num: 7600
num of homozygotes: 0

Other
type: Population
allele count: 81
allele frequency: 1.033163265306122e-1
allele num: 784
num of homozygotes: 0

Latino
type: Population
allele count: 673
allele frequency: 7.245908699397072e-2
allele num: 9288
num of homozygotes: 0

South Asian
type: Population
allele count: 1056
allele frequency: 7.45446844557391e-2
allele num: 14166
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.362e-1

FS
type: SiteQuality
SIO_000300: 1.5567e1

QD
type: SiteQuality
SIO_000300: 1.67e0

MQRankSum
type: SiteQuality
SIO_000300: -3.353e0

DP
type: SiteQuality
SIO_000300: 5.782703e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

MQ
type: SiteQuality
SIO_000300: 3.942e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.6e-1

GenotypeQuality
all individuals: 339
bin: 5.25e1
variant carriers: 54

GenotypeQuality
all individuals: 978
bin: 2.25e1
variant carriers: 63

GenotypeQuality
all individuals: 2016
bin: 6.25e1
variant carriers: 47

GenotypeQuality
all individuals: 390
bin: 2.75e1
variant carriers: 73

GenotypeQuality
all individuals: 1839
bin: 7.75e1
variant carriers: 36

GenotypeQuality
all individuals: 339
bin: 3.75e1
variant carriers: 63

South Asian
type: Population
allele count: 79
allele frequency: 4.832986663403891e-3
allele num: 16346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 763
allele frequency: 1.192112992937941e-2
allele num: 64004
num of homozygotes: 0

Other
type: Population
allele count: 16
allele frequency: 1.830663615560641e-2
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 50
allele frequency: 4.368338284116722e-3
allele num: 11446
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.320724065908564e-4
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 283
allele frequency: 3.120176405733186e-2
allele num: 9070
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 147
allele frequency: 2.29043315674665e-2
allele num: 6418
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.044e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.77e-2

FS
type: SiteQuality
SIO_000300: 2.5205e1

MQ
type: SiteQuality
SIO_000300: 3.868e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.274e0

DP
type: SiteQuality
SIO_000300: 5.333102e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.775e0

QD
type: SiteQuality
SIO_000300: 8.100000000000001e-1

GenotypeQuality
all individuals: 1776
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1750
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1654
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1869
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.064946210194011e-5
allele num: 65254
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
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: 900
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

DP
type: SiteQuality
SIO_000300: 5.197792e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.096e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.620000000000001e-1

MQ
type: SiteQuality
SIO_000300: 3.999e1

FS
type: SiteQuality
SIO_000300: 4.0876e1

MQRankSum
type: SiteQuality
SIO_000300: -2.519e0

QD
type: SiteQuality
SIO_000300: 9.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.542e0

GenotypeQuality
all individuals: 45088
bin: 9.75e1
variant carriers: 190

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 8

GenotypeQuality
all individuals: 162
bin: 2.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1907
bin: 8.25e1
variant carriers: 9

GenotypeQuality
all individuals: 1681
bin: 7.25e1
variant carriers: 9

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 10

Latino
type: Population
allele count: 15
allele frequency: 1.301631377993752e-3
allele num: 11524
num of homozygotes: 0

South Asian
type: Population
allele count: 37
allele frequency: 2.258576486387498e-3
allele num: 16382
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.278772378516624e-3
allele num: 8602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 147
allele frequency: 2.260912362730321e-3
allele num: 65018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.062443164595332e-4
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 129
allele frequency: 1.401260047794916e-2
allele num: 9206
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.222222222222222e-3
allele num: 900
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 3.893e1

VQSLOD
type: SiteQuality
SIO_000300: -2.074e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.822e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

FS
type: SiteQuality
SIO_000300: 3.184e0

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.168e0

DP
type: SiteQuality
SIO_000300: 5.198044e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.88e-1

GenotypeQuality
all individuals: 1648
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46003
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 578
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1774
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9470
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65274
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

FS
type: SiteQuality
SIO_000300: 1.976e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 3.884e1

DP
type: SiteQuality
SIO_000300: 5.165746e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.766e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

QD
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
all individuals: 167
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45961
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1780
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.11595429538722e-4
allele num: 9452
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532285250222181e-5
allele num: 65262
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: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.033e0

DP
type: SiteQuality
SIO_000300: 5.164775e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.274e0

MQ
type: SiteQuality
SIO_000300: 3.884e1

VQSLOD
type: SiteQuality
SIO_000300: -5.098e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

FS
type: SiteQuality
SIO_000300: 2.0427e1

QD
type: SiteQuality
SIO_000300: 1.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.54e-1

GenotypeQuality
all individuals: 1894
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1774
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45976
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9368
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.607304112786805e-5
allele num: 65114
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.115e0

DP
type: SiteQuality
SIO_000300: 5.163077e6

QD
type: SiteQuality
SIO_000300: 6.0e-2

FS
type: SiteQuality
SIO_000300: 2.0984e1

MQ
type: SiteQuality
SIO_000300: 3.929e1

VQSLOD
type: SiteQuality
SIO_000300: -5.263e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.154e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

GenotypeQuality
all individuals: 602
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.070434596446157e-4
allele num: 9342
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
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: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65062
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.166e0

MQ
type: SiteQuality
SIO_000300: 3.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 4.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

DP
type: SiteQuality
SIO_000300: 5.162508e6

FS
type: SiteQuality
SIO_000300: 1.7903e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.38e-1

GenotypeQuality
all individuals: 2461
bin: 6.25e1
variant carriers: 240

GenotypeQuality
all individuals: 1637
bin: 7.5e0
variant carriers: 442

GenotypeQuality
all individuals: 2226
bin: 8.25e1
variant carriers: 141

GenotypeQuality
all individuals: 26535
bin: 9.75e1
variant carriers: 1244

GenotypeQuality
all individuals: 2173
bin: 7.25e1
variant carriers: 162

GenotypeQuality
all individuals: 2365
bin: 6.75e1
variant carriers: 162

Latino
type: Population
allele count: 529
allele frequency: 5.107163545085924e-2
allele num: 10358
num of homozygotes: 0

East Asian
type: Population
allele count: 402
allele frequency: 5.290866017372993e-2
allele num: 7598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 317
allele frequency: 5.459869100930072e-2
allele num: 5806
num of homozygotes: 0

South Asian
type: Population
allele count: 492
allele frequency: 3.214005748628168e-2
allele num: 15308
num of homozygotes: 0

Other
type: Population
allele count: 37
allele frequency: 4.447115384615385e-2
allele num: 832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2435
allele frequency: 4.177818955459475e-2
allele num: 58284
num of homozygotes: 0

African
type: Population
allele count: 305
allele frequency: 3.658829174664108e-2
allele num: 8336
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.557e0

DP
type: SiteQuality
SIO_000300: 5.072505e6

MQ
type: SiteQuality
SIO_000300: 3.864e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.75e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 2.7558e1

QD
type: SiteQuality
SIO_000300: 5.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.312e0

GenotypeQuality
all individuals: 2226
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2061
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2365
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5806
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.532532009406845e-5
allele num: 15308
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7598
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.47e-1

DP
type: SiteQuality
SIO_000300: 5.072505e6

MQ
type: SiteQuality
SIO_000300: 3.864e1

MQRankSum
type: SiteQuality
SIO_000300: -2.557e0

FS
type: SiteQuality
SIO_000300: 2.7558e1

QD
type: SiteQuality
SIO_000300: 5.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.312e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: -5.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.75e-2

GenotypeQuality
all individuals: 47560
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1599
bin: 9.25e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817520901490367e-4
allele num: 16506
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64946
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.9418e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 3.836e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.91e-1

QD
type: SiteQuality
SIO_000300: 2.4e-1

DP
type: SiteQuality
SIO_000300: 4.945657e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.845e0

VQSLOD
type: SiteQuality
SIO_000300: -4.861e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.559e0

GenotypeQuality
all individuals: 1422
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28698
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1342
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1515
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5754
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9676
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.161271841879118e-5
allele num: 13964
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.63253296523666e-5
allele num: 55058
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7006
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.543e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.97e0

MQRankSum
type: SiteQuality
SIO_000300: -3.513e0

FS
type: SiteQuality
SIO_000300: 5.749e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

MQ
type: SiteQuality
SIO_000300: 3.902e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.88e-1

DP
type: SiteQuality
SIO_000300: 5.022083e6

QD
type: SiteQuality
SIO_000300: 2.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.995e-1

GenotypeQuality
all individuals: 1468
bin: 2.75e1
variant carriers: 611

GenotypeQuality
all individuals: 1342
bin: 8.75e1
variant carriers: 572

GenotypeQuality
all individuals: 1574
bin: 6.75e1
variant carriers: 550

GenotypeQuality
all individuals: 1422
bin: 7.75e1
variant carriers: 547

GenotypeQuality
all individuals: 1382
bin: 8.25e1
variant carriers: 570

GenotypeQuality
all individuals: 1379
bin: 4.25e1
variant carriers: 600

South Asian
type: Population
allele count: 4344
allele frequency: 3.110856488112289e-1
allele num: 13964
num of homozygotes: 0

Other
type: Population
allele count: 243
allele frequency: 3.292682926829268e-1
allele num: 738
num of homozygotes: 0

East Asian
type: Population
allele count: 1840
allele frequency: 2.626320296888381e-1
allele num: 7006
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2051
allele frequency: 3.564476885644769e-1
allele num: 5754
num of homozygotes: 0

Latino
type: Population
allele count: 2973
allele frequency: 3.072550640760645e-1
allele num: 9676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19242
allele frequency: 3.49485996585419e-1
allele num: 55058
num of homozygotes: 0

African
type: Population
allele count: 1318
allele frequency: 1.760149572649573e-1
allele num: 7488
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.022083e6

QD
type: SiteQuality
SIO_000300: 2.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.995e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.513e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.543e1

FS
type: SiteQuality
SIO_000300: 5.749e0

MQ
type: SiteQuality
SIO_000300: 3.902e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.97e0

GenotypeQuality
all individuals: 100
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2489
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2382
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2556
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.082994203970897e-5
allele num: 64872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9192
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: 8624
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 3.882e1

QD
type: SiteQuality
SIO_000300: 3.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.108e0

MQRankSum
type: SiteQuality
SIO_000300: -1.168e0

FS
type: SiteQuality
SIO_000300: 1.4689e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.859e0

DP
type: SiteQuality
SIO_000300: 3.804684e6

GenotypeQuality
all individuals: 40568
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2381
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3345
bin: 6.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9184
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64880
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 5.95e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.804022e6

VQSLOD
type: SiteQuality
SIO_000300: -3.141e0

MQ
type: SiteQuality
SIO_000300: 3.93e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.86e-1

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

GenotypeQuality
all individuals: 2347
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2555
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2130
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2380
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 7
allele frequency: 7.615317667536989e-4
allele num: 9192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64874
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 80
allele frequency: 9.278589654372536e-3
allele num: 8622
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -4.47e0

QD
type: SiteQuality
SIO_000300: 6.77e0

MQ
type: SiteQuality
SIO_000300: 3.992e1

DP
type: SiteQuality
SIO_000300: 3.80384e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.69e0

FS
type: SiteQuality
SIO_000300: 1.5678e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

GenotypeQuality
all individuals: 3273
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2346
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40536
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
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variant carriers: 0

GenotypeQuality
all individuals: 2484
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9164
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: 0
allele frequency: 0.0e0
allele num: 64810
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 8.195e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.666e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 3.9e1

MQRankSum
type: SiteQuality
SIO_000300: -1.428e0

QD
type: SiteQuality
SIO_000300: 2.61e0

VQSLOD
type: SiteQuality
SIO_000300: -3.367e0

DP
type: SiteQuality
SIO_000300: 3.800249e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

GenotypeQuality
all individuals: 120
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2556
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40535
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64816
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: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.090750436300175e-4
allele num: 9168
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.732e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 4.068e1

MQRankSum
type: SiteQuality
SIO_000300: -1.115e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.05e-1

QD
type: SiteQuality
SIO_000300: 7.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.850000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.599e0

DP
type: SiteQuality
SIO_000300: 3.79975e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.19e-1

GenotypeQuality
all individuals: 688
bin: 4.75e1
variant carriers: 70

GenotypeQuality
all individuals: 2539
bin: 7.75e1
variant carriers: 36

GenotypeQuality
all individuals: 33002
bin: 9.75e1
variant carriers: 398

GenotypeQuality
all individuals: 2258
bin: 8.75e1
variant carriers: 40

GenotypeQuality
all individuals: 2446
bin: 8.25e1
variant carriers: 33

GenotypeQuality
all individuals: 3499
bin: 6.25e1
variant carriers: 63

European (Non-Finnish)
type: Population
allele count: 668
allele frequency: 1.070272695228635e-2
allele num: 62414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 78
allele frequency: 1.24124761298536e-2
allele num: 6284
num of homozygotes: 0

African
type: Population
allele count: 187
allele frequency: 2.207271010387158e-2
allele num: 8472
num of homozygotes: 0

East Asian
type: Population
allele count: 49
allele frequency: 5.783758262511804e-3
allele num: 8472
num of homozygotes: 0

South Asian
type: Population
allele count: 308
allele frequency: 1.940524193548387e-2
allele num: 15872
num of homozygotes: 0

Latino
type: Population
allele count: 70
allele frequency: 6.234413965087282e-3
allele num: 11228
num of homozygotes: 0

Other
type: Population
allele count: 21
allele frequency: 2.430555555555556e-2
allele num: 864
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.08e-1

FS
type: SiteQuality
SIO_000300: 2.0171e1

MQRankSum
type: SiteQuality
SIO_000300: -1.777e0

MQ
type: SiteQuality
SIO_000300: 4.06e1

DP
type: SiteQuality
SIO_000300: 3.785609e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.238e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.073e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.523e0

QD
type: SiteQuality
SIO_000300: 7.0e-1

GenotypeQuality
all individuals: 688
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3499
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2491
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.180358829084042e-4
allele num: 8472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62414
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6284
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.073e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.08e-1

DP
type: SiteQuality
SIO_000300: 3.785609e6

MQRankSum
type: SiteQuality
SIO_000300: -1.777e0

MQ
type: SiteQuality
SIO_000300: 4.06e1

FS
type: SiteQuality
SIO_000300: 2.0171e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.523e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.238e0

QD
type: SiteQuality
SIO_000300: 7.0e-1

GenotypeQuality
all individuals: 2328
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 165
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 38689
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2551
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.088613106901807e-4
allele num: 9186
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.337265787647467e-4
allele num: 11528
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: 8
allele frequency: 1.236743653959126e-4
allele num: 64686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.518833535844471e-4
allele num: 6584
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.213150551983501e-4
allele num: 16486
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.949e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -5.977e0

FS
type: SiteQuality
SIO_000300: 1.5429e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

MQ
type: SiteQuality
SIO_000300: 4.16e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.679e0

MQRankSum
type: SiteQuality
SIO_000300: -1.223e0

DP
type: SiteQuality
SIO_000300: 3.713562e6

QD
type: SiteQuality
SIO_000300: 1.1e-1

GenotypeQuality
all individuals: 3519
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2957
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2712
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 137
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39024
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.082614056720099e-5
allele num: 64880
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 4.933e1

MQRankSum
type: SiteQuality
SIO_000300: 3.39e0

QD
type: SiteQuality
SIO_000300: 1.042e1

FS
type: SiteQuality
SIO_000300: 7.185e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.638e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.831e0

DP
type: SiteQuality
SIO_000300: 3.71071e6

GenotypeQuality
all individuals: 879
bin: 4.25e1
variant carriers: 68

GenotypeQuality
all individuals: 2583
bin: 7.25e1
variant carriers: 39

GenotypeQuality
all individuals: 2581
bin: 7.75e1
variant carriers: 38

GenotypeQuality
all individuals: 2849
bin: 6.75e1
variant carriers: 32

GenotypeQuality
all individuals: 1018
bin: 5.25e1
variant carriers: 55

GenotypeQuality
all individuals: 2462
bin: 8.25e1
variant carriers: 26

European (Finnish)
type: Population
allele count: 65
allele frequency: 1.073670300627684e-2
allele num: 6054
num of homozygotes: 0

African
type: Population
allele count: 35
allele frequency: 3.96286231884058e-3
allele num: 8832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 751
allele frequency: 1.320184228105334e-2
allele num: 56886
num of homozygotes: 0

Latino
type: Population
allele count: 110
allele frequency: 1.066098081023454e-2
allele num: 10318
num of homozygotes: 0

South Asian
type: Population
allele count: 65
allele frequency: 4.052369077306733e-3
allele num: 16040
num of homozygotes: 0

East Asian
type: Population
allele count: 21
allele frequency: 2.551640340218712e-3
allele num: 8230
num of homozygotes: 0

Other
type: Population
allele count: 12
allele frequency: 1.477832512315271e-2
allele num: 812
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.735117e6

MQRankSum
type: SiteQuality
SIO_000300: -2.334e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

VQSLOD
type: SiteQuality
SIO_000300: -2.94e0

FS
type: SiteQuality
SIO_000300: 2.004e0

MQ
type: SiteQuality
SIO_000300: 4.259e1

QD
type: SiteQuality
SIO_000300: 7.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.27e-2

GenotypeQuality
all individuals: 2240
bin: 8.75e1
variant carriers: 48

GenotypeQuality
all individuals: 3048
bin: 6.75e1
variant carriers: 79

GenotypeQuality
all individuals: 919
bin: 4.75e1
variant carriers: 106

GenotypeQuality
all individuals: 946
bin: 5.25e1
variant carriers: 119

GenotypeQuality
all individuals: 2528
bin: 8.25e1
variant carriers: 57

GenotypeQuality
all individuals: 2692
bin: 7.75e1
variant carriers: 72

South Asian
type: Population
allele count: 412
allele frequency: 2.63764404609475e-2
allele num: 15620
num of homozygotes: 0

East Asian
type: Population
allele count: 181
allele frequency: 2.235671936758893e-2
allele num: 8096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 528
allele frequency: 8.418904266853754e-3
allele num: 62716
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 85
allele frequency: 1.33816120906801e-2
allele num: 6352
num of homozygotes: 0

African
type: Population
allele count: 491
allele frequency: 5.937122128174124e-2
allele num: 8270
num of homozygotes: 0

Latino
type: Population
allele count: 199
allele frequency: 1.817351598173516e-2
allele num: 10950
num of homozygotes: 0

Other
type: Population
allele count: 12
allele frequency: 1.392111368909513e-2
allele num: 862
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.926e0

QD
type: SiteQuality
SIO_000300: 7.2e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.033e0

VQSLOD
type: SiteQuality
SIO_000300: -7.085e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.076e0

DP
type: SiteQuality
SIO_000300: 3.635e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-2

FS
type: SiteQuality
SIO_000300: 2.0237e1

MQ
type: SiteQuality
SIO_000300: 4.297e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-1

GenotypeQuality
all individuals: 2320
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39546
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2040
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540072691431036e-5
allele num: 64932
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9238
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.572e0

FS
type: SiteQuality
SIO_000300: 4.08e0

DP
type: SiteQuality
SIO_000300: 3.595706e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

VQSLOD
type: SiteQuality
SIO_000300: -2.429e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.62e0

QD
type: SiteQuality
SIO_000300: 1.092e1

MQ
type: SiteQuality
SIO_000300: 4.555e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

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

GenotypeQuality
all individuals: 2319
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2888
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2531
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4204
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 43
allele frequency: 6.621496766245766e-4
allele num: 64940
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9246
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.724e0

MQ
type: SiteQuality
SIO_000300: 4.389e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e-1

FS
type: SiteQuality
SIO_000300: 4.158e0

QD
type: SiteQuality
SIO_000300: 9.369999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

DP
type: SiteQuality
SIO_000300: 3.595907e6

MQRankSum
type: SiteQuality
SIO_000300: 1.78e0

VQSLOD
type: SiteQuality
SIO_000300: -1.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.06e-1

GenotypeQuality
all individuals: 1845
bin: 3.25e1
variant carriers: 740

GenotypeQuality
all individuals: 1347
bin: 8.75e1
variant carriers: 557

GenotypeQuality
all individuals: 1842
bin: 7.75e1
variant carriers: 658

GenotypeQuality
all individuals: 1382
bin: 9.25e1
variant carriers: 556

GenotypeQuality
all individuals: 1670
bin: 5.75e1
variant carriers: 666

GenotypeQuality
all individuals: 1835
bin: 1.75e1
variant carriers: 681

European (Non-Finnish)
type: Population
allele count: 13083
allele frequency: 2.422598326049922e-1
allele num: 54004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1819
allele frequency: 3.285765895953757e-1
allele num: 5536
num of homozygotes: 0

African
type: Population
allele count: 2655
allele frequency: 3.413473900745693e-1
allele num: 7778
num of homozygotes: 0

South Asian
type: Population
allele count: 3754
allele frequency: 2.66430092264017e-1
allele num: 14090
num of homozygotes: 0

Latino
type: Population
allele count: 3029
allele frequency: 3.128485850030985e-1
allele num: 9682
num of homozygotes: 0

East Asian
type: Population
allele count: 2109
allele frequency: 2.952127659574468e-1
allele num: 7144
num of homozygotes: 0

Other
type: Population
allele count: 210
allele frequency: 2.74869109947644e-1
allele num: 764
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.836e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.211e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.354e0

VQSLOD
type: SiteQuality
SIO_000300: 2.855e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.07e-1

MQ
type: SiteQuality
SIO_000300: 4.441e1

FS
type: SiteQuality
SIO_000300: 2.7653e1

QD
type: SiteQuality
SIO_000300: 2.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.342e-1

DP
type: SiteQuality
SIO_000300: 3.648806e6

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2752
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4059
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4185
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 3.69321679182568e-4
allele num: 64984
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.730403183941858e-4
allele num: 11558
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.158428663932657e-4
allele num: 9266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

FS
type: SiteQuality
SIO_000300: 6.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

QD
type: SiteQuality
SIO_000300: 8.710000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.165e0

MQ
type: SiteQuality
SIO_000300: 4.646e1

DP
type: SiteQuality
SIO_000300: 2.613482e6

GenotypeQuality
all individuals: 164
bin: 1.25e1
variant carriers: 9

GenotypeQuality
all individuals: 2251
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 303
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 4947
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4059
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 23983
bin: 9.75e1
variant carriers: 32

European (Non-Finnish)
type: Population
allele count: 36
allele frequency: 5.607826032774627e-4
allele num: 64196
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.45218945487042e-3
allele num: 8952
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.744316194473592e-4
allele num: 11436
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.060484819957637e-4
allele num: 8498
num of homozygotes: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.11358574610245e-3
allele num: 16164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.059039461609055e-4
allele num: 6538
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.41e-1

MQ
type: SiteQuality
SIO_000300: 4.774e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

MQRankSum
type: SiteQuality
SIO_000300: -2.213e0

QD
type: SiteQuality
SIO_000300: 9.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.72e-1

FS
type: SiteQuality
SIO_000300: 1.3109e1

DP
type: SiteQuality
SIO_000300: 2.621885e6

VQSLOD
type: SiteQuality
SIO_000300: -3.017e0

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25255
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1442
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2345
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4981
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
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: 9
allele frequency: 1.386150813208477e-4
allele num: 64928
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.559e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 9.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQ
type: SiteQuality
SIO_000300: 4.933e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.89e-1

DP
type: SiteQuality
SIO_000300: 2.559956e6

GenotypeQuality
all individuals: 2346
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4752
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4170
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25245
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542971763616726e-5
allele num: 64810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9232
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.315e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

MQ
type: SiteQuality
SIO_000300: 5.176e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.03e0

QD
type: SiteQuality
SIO_000300: 7.11e0

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

DP
type: SiteQuality
SIO_000300: 2.543114e6

GenotypeQuality
all individuals: 374
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4243
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4738
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64812
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9238
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.171508903467666e-4
allele num: 8536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.54083e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

QD
type: SiteQuality
SIO_000300: 8.75e0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

FS
type: SiteQuality
SIO_000300: 1.411e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

MQ
type: SiteQuality
SIO_000300: 5.322e1

GenotypeQuality
all individuals: 564
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4244
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64778
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9226
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.312e1

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.478e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.0e-1

FS
type: SiteQuality
SIO_000300: 2.699e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

DP
type: SiteQuality
SIO_000300: 2.537334e6

MQ
type: SiteQuality
SIO_000300: 5.472e1

GenotypeQuality
all individuals: 2393
bin: 4.25e1
variant carriers: 642

GenotypeQuality
all individuals: 5524
bin: 6.25e1
variant carriers: 530

GenotypeQuality
all individuals: 1383
bin: 7.75e1
variant carriers: 448

GenotypeQuality
all individuals: 2647
bin: 3.25e1
variant carriers: 753

GenotypeQuality
all individuals: 1190
bin: 8.25e1
variant carriers: 430

European (Non-Finnish)
type: Population
allele count: 7885
allele frequency: 1.66694854340197e-1
allele num: 47302
num of homozygotes: 0

South Asian
type: Population
allele count: 2387
allele frequency: 1.922829063960045e-1
allele num: 12414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1120
allele frequency: 2.313093762907889e-1
allele num: 4842
num of homozygotes: 0

Other
type: Population
allele count: 135
allele frequency: 2.039274924471299e-1
allele num: 662
num of homozygotes: 0

East Asian
type: Population
allele count: 908
allele frequency: 1.402100061766522e-1
allele num: 6476
num of homozygotes: 0

Latino
type: Population
allele count: 1508
allele frequency: 1.761270731137585e-1
allele num: 8562
num of homozygotes: 0

African
type: Population
allele count: 1256
allele frequency: 1.835720549546916e-1
allele num: 6842
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.688e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.568e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.65e-1

QD
type: SiteQuality
SIO_000300: 2.34e0

FS
type: SiteQuality
SIO_000300: 1.7706e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

MQ
type: SiteQuality
SIO_000300: 5.211e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-2

DP
type: SiteQuality
SIO_000300: 2.489491e6

GenotypeQuality
all individuals: 4005
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2069
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4842
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6842
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.114075514777388e-5
allele num: 47302
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12414
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.0e0

QD
type: SiteQuality
SIO_000300: 2.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.65e-1

DP
type: SiteQuality
SIO_000300: 2.489491e6

FS
type: SiteQuality
SIO_000300: 1.7706e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.688e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.568e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

MQ
type: SiteQuality
SIO_000300: 5.211e1

GenotypeQuality
all individuals: 21785
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4805
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.195594932003346e-5
allele num: 64562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

FS
type: SiteQuality
SIO_000300: 2.5432e1

VQSLOD
type: SiteQuality
SIO_000300: -5.486e0

QD
type: SiteQuality
SIO_000300: 3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.073e0

MQ
type: SiteQuality
SIO_000300: 5.146e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.764e0

DP
type: SiteQuality
SIO_000300: 2.024221e6

GenotypeQuality
all individuals: 9127
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21644
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7580
bin: 9.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64558
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: 8478
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.644e0

DP
type: SiteQuality
SIO_000300: 2.020068e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.644e0

QD
type: SiteQuality
SIO_000300: 1.871e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.51e-1

MQ
type: SiteQuality
SIO_000300: 5.327e1

VQSLOD
type: SiteQuality
SIO_000300: 3.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

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

GenotypeQuality
all individuals: 3754
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8828
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9128
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554194771688788e-5
allele num: 64342
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.922e0

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.164e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.198e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.182e1

QD
type: SiteQuality
SIO_000300: 1.345e1

DP
type: SiteQuality
SIO_000300: 1.988382e6

GenotypeQuality
all individuals: 2543
bin: 4.25e1
variant carriers: 35

GenotypeQuality
all individuals: 1611
bin: 5.75e1
variant carriers: 25

GenotypeQuality
all individuals: 1591
bin: 8.25e1
variant carriers: 15

GenotypeQuality
all individuals: 2646
bin: 7.5e0
variant carriers: 51

GenotypeQuality
all individuals: 7062
bin: 6.25e1
variant carriers: 29

Other
type: Population
allele count: 5
allele frequency: 6.944444444444444e-3
allele num: 720
num of homozygotes: 0

African
type: Population
allele count: 75
allele frequency: 1.109467455621302e-2
allele num: 6760
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 37
allele frequency: 6.892697466467959e-3
allele num: 5368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 259
allele frequency: 4.896030245746692e-3
allele num: 52900
num of homozygotes: 0

Latino
type: Population
allele count: 30
allele frequency: 3.2481593763534e-3
allele num: 9236
num of homozygotes: 0

South Asian
type: Population
allele count: 168
allele frequency: 1.328483314882176e-2
allele num: 12646
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 1.70261066969353e-3
allele num: 7048
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.92e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.922e0

MQ
type: SiteQuality
SIO_000300: 5.073e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

FS
type: SiteQuality
SIO_000300: 8.669e0

VQSLOD
type: SiteQuality
SIO_000300: -2.467e0

DP
type: SiteQuality
SIO_000300: 1.878748e6

QD
type: SiteQuality
SIO_000300: 1.55e0

GenotypeQuality
all individuals: 1611
bin: 5.75e1
variant carriers: 146

GenotypeQuality
all individuals: 1591
bin: 8.25e1
variant carriers: 135

GenotypeQuality
all individuals: 910
bin: 8.75e1
variant carriers: 111

GenotypeQuality
all individuals: 3794
bin: 6.75e1
variant carriers: 184

GenotypeQuality
all individuals: 2317
bin: 5.25e1
variant carriers: 204

South Asian
type: Population
allele count: 873
allele frequency: 6.90336865411988e-2
allele num: 12646
num of homozygotes: 0

East Asian
type: Population
allele count: 278
allele frequency: 3.944381384790011e-2
allele num: 7048
num of homozygotes: 0

African
type: Population
allele count: 450
allele frequency: 6.656804733727811e-2
allele num: 6760
num of homozygotes: 0

Other
type: Population
allele count: 34
allele frequency: 4.722222222222222e-2
allele num: 720
num of homozygotes: 0

Latino
type: Population
allele count: 411
allele frequency: 4.449978345604157e-2
allele num: 9236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 221
allele frequency: 4.11698956780924e-2
allele num: 5368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1563
allele frequency: 2.954631379962193e-2
allele num: 52900
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.073e1

DP
type: SiteQuality
SIO_000300: 1.878748e6

MQRankSum
type: SiteQuality
SIO_000300: -2.922e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.92e-1

FS
type: SiteQuality
SIO_000300: 8.669e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

VQSLOD
type: SiteQuality
SIO_000300: -2.467e0

QD
type: SiteQuality
SIO_000300: 1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.9e-3

GenotypeQuality
all individuals: 1547
bin: 2.5e0
variant carriers: 48

GenotypeQuality
all individuals: 3185
bin: 4.75e1
variant carriers: 37

GenotypeQuality
all individuals: 1589
bin: 9.25e1
variant carriers: 15

GenotypeQuality
all individuals: 3529
bin: 3.75e1
variant carriers: 63

GenotypeQuality
all individuals: 3380
bin: 7.75e1
variant carriers: 26

European (Finnish)
type: Population
allele count: 40
allele frequency: 6.426735218508998e-3
allele num: 6224
num of homozygotes: 0

South Asian
type: Population
allele count: 73
allele frequency: 4.655612244897959e-3
allele num: 15680
num of homozygotes: 0

Latino
type: Population
allele count: 58
allele frequency: 5.361434645960436e-3
allele num: 10818
num of homozygotes: 0

African
type: Population
allele count: 25
allele frequency: 2.913073875553484e-3
allele num: 8582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 465
allele frequency: 7.799919484702093e-3
allele num: 59616
num of homozygotes: 0

East Asian
type: Population
allele count: 23
allele frequency: 2.854306279473815e-3
allele num: 8058
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 7.058823529411765e-3
allele num: 850
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.661e0

VQSLOD
type: SiteQuality
SIO_000300: -2.183e0

QD
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 5.112e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 1.815903e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.71e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.815e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.01e-1

GenotypeQuality
all individuals: 1701
bin: 4.25e1
variant carriers: 324

GenotypeQuality
all individuals: 1137
bin: 6.75e1
variant carriers: 355

GenotypeQuality
all individuals: 3095
bin: 3.25e1
variant carriers: 411

GenotypeQuality
all individuals: 500
bin: 9.25e1
variant carriers: 227

GenotypeQuality
all individuals: 3838
bin: 2.25e1
variant carriers: 423

African
type: Population
allele count: 1085
allele frequency: 2.217906786590352e-1
allele num: 4892
num of homozygotes: 0

South Asian
type: Population
allele count: 1887
allele frequency: 2.140912185159973e-1
allele num: 8814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 782
allele frequency: 2.150715071507151e-1
allele num: 3636
num of homozygotes: 0

Latino
type: Population
allele count: 940
allele frequency: 1.653764954257565e-1
allele num: 5684
num of homozygotes: 0

Other
type: Population
allele count: 95
allele frequency: 1.9e-1
allele num: 500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5049
allele frequency: 1.492374083707732e-1
allele num: 33832
num of homozygotes: 0

East Asian
type: Population
allele count: 666
allele frequency: 1.488600804649084e-1
allele num: 4474
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 1.741583e6

VQSLOD
type: SiteQuality
SIO_000300: 1.266e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.225e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

MQRankSum
type: SiteQuality
SIO_000300: -3.249e0

MQ
type: SiteQuality
SIO_000300: 5.089e1

FS
type: SiteQuality
SIO_000300: 1.1169e1

QD
type: SiteQuality
SIO_000300: 4.1e0

GenotypeQuality
all individuals: 1018
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1775
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3820
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4530
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1737
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62668
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16142
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.671970624235006e-4
allele num: 8170
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8746
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

FS
type: SiteQuality
SIO_000300: 1.373e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.909e0

MQ
type: SiteQuality
SIO_000300: 5.285e1

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 1.53295e6

QD
type: SiteQuality
SIO_000300: 7.27e0

GenotypeQuality
all individuals: 3103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2634
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1775
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16712
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.857395925597875e-5
allele num: 11290
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16142
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.373e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.909e0

DP
type: SiteQuality
SIO_000300: 1.53295e6

QD
type: SiteQuality
SIO_000300: 7.27e0

MQ
type: SiteQuality
SIO_000300: 5.285e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

GenotypeQuality
all individuals: 2467
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5125
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5720
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3831
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 5419
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8716
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11284
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.202453987730061e-4
allele num: 6520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.921045048506387e-4
allele num: 62466
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

MQ
type: SiteQuality
SIO_000300: 5.279e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

FS
type: SiteQuality
SIO_000300: 1.845e0

VQSLOD
type: SiteQuality
SIO_000300: -1.228e0

DP
type: SiteQuality
SIO_000300: 1.50412e6

QD
type: SiteQuality
SIO_000300: 1.149e1

GenotypeQuality
all individuals: 3063
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1710
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5720
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11863
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.862105636299185e-5
allele num: 11284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8716
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16154
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

QD
type: SiteQuality
SIO_000300: 1.149e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

DP
type: SiteQuality
SIO_000300: 1.50412e6

MQRankSum
type: SiteQuality
SIO_000300: 9.07e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.228e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQ
type: SiteQuality
SIO_000300: 5.279e1

FS
type: SiteQuality
SIO_000300: 1.845e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0