4-77018807-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018807
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018807
    reference: chr 4
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.210C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.792C>T
  hgvsp: ENST00000349321.3:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3141C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.792C>T
  hgvsp: ENST00000355810.4:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.48C>T
  hgvsp: ENST00000511188.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.89C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1301C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.792C>T
  hgvsp: ENST00000341029.5:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1301C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.908C>T
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8932
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr264Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

4-77018808-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018808
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018808
    reference: chr 4
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1300G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.909G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.793G>A
  hgvsp: ENSP00000348064.4:p.Glu265Lys
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.90G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.211G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.793G>A
  hgvsp: ENSP00000343843.5:p.Glu265Lys
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.49G>A
  hgvsp: ENSP00000422249.1:p.Glu17Lys
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1300G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3140G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.793G>A
  hgvsp: ENSP00000304313.5:p.Glu265Lys
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu265Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

4-77018819-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018819
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018819
    reference: chr 4
allele count: 2
allele frequency: 1.65371258475277e-5
allele num: 120940
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1289T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.804T>G
  hgvsp: ENSP00000304313.5:p.Ile268Met
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3129T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.222T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.804T>G
  hgvsp: ENSP00000343843.5:p.Ile268Met
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.804T>G
  hgvsp: ENSP00000348064.4:p.Ile268Met
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.60T>G
  hgvsp: ENSP00000422249.1:p.Ile20Met
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.920T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.101T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1289T>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6228
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile268Met
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/4-77018825-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018825
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018825
    reference: chr 4
allele count: 1
allele frequency: 8.270751315049459e-6
allele num: 120908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.66C>A
  hgvsp: ENSP00000422249.1:p.Asn22Lys
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.810C>A
  hgvsp: ENSP00000348064.4:p.Asn270Lys
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.107C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.810C>A
  hgvsp: ENSP00000343843.5:p.Asn270Lys
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.926C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1283C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.810C>A
  hgvsp: ENSP00000304313.5:p.Asn270Lys
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1283C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.228C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3123C>A
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn270Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

4-77018832-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018832
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018832
    reference: chr 4
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1276A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1276A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+3A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+3A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+3A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+3A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3116A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+3A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+3A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+3A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
hgvs: c.814+3A>G
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/4-77018837-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018837
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018838
    reference: chr 4
allele count: 3
allele frequency: 2.482005460412013e-5
allele num: 120870
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+8_814+9insC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1271_38-1270insC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+8_930+9insC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+8_232+9insC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3111_79-3110insC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+8_111+9insC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+8_70+9insC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1271_79-1270insC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+8_814+9insC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+8_814+9insC
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2722
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ

4-77018838-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018838
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018838
    reference: chr 4
allele count: 2
allele frequency: 1.65508109897385e-5
allele num: 120840
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+9G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+9G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+9G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1270G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3110G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+9G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+9G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1270G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+9G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+9G>T
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5979
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2225
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8638
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum

4-77018843-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018843
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018843
    reference: chr 4
allele count: 3
allele frequency: 2.483690432824453e-5
allele num: 120788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+14A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1265A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+14A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+14A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3105A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+14A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+14A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1265A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+14A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+14A>T
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8454
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-77018851-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018851
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018851
    reference: chr 4
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1257A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+22A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+22A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1257A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+22A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+22A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+22A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+22A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3097A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+22A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7762
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum

4-77018857-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018857
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018857
    reference: chr 4
allele count: 6
allele frequency: 4.973227458846543e-5
allele num: 120646
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1251A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3091A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1251A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+28A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1374
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

4-77018858-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018858
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018858
    reference: chr 4
allele count: 1
allele frequency: 8.290361625574107e-6
allele num: 120622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+29T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+29T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+29T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1250T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+29T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1250T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+29T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3090T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+29T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+29T>A
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-77018861-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018861
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018861
    reference: chr 4
allele count: 1
allele frequency: 8.292148993333113e-6
allele num: 120596
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+32T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+32T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+32T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+32T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+32T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+32T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3087T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1247T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+32T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1247T>C
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1371
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

4-77018862-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018862
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018862
    reference: chr 4
allele count: 1
allele frequency: 8.291598951941893e-6
allele num: 120604
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3086A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1246A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+33A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+33A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+33A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+33A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+33A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1246A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+33A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+33A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2401
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

4-77018868-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018868
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018868
    reference: chr 4
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+39T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1240T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3080T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+39T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1240T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+39T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+39T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+39T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+39T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+39T>A
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5976
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  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: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

4-77018869-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018869
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018869
    reference: chr 4
allele count: 2
allele frequency: 1.659695943703114e-5
allele num: 120504
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+40T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1239T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3079T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+40T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+40T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+40T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+40T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+40T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1239T>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+40T>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2721
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

4-77018871-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018871
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018871
    reference: chr 4
allele count: 1
allele frequency: 8.299995020002988e-6
allele num: 120482
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1237A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+42A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+42A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+42A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3077A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+42A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+42A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+42A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1237A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+42A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5978
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5286
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2721
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-77018874-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018874
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018874
    reference: chr 4
allele count: 19
allele frequency: 1.577942031392741e-4
allele num: 120410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3074A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1234A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+45A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+45A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+45A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+45A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+45A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+45A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+45A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1234A>C
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5967
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2202
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38536
  bin: 9.75e1
  variant carriers: 19
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

4-77018874-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018874
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018874
    reference: chr 4
allele count: 54
allele frequency: 4.48467735237937e-4
allele num: 120410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+45A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+45A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3074A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1234A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1234A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+45A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+45A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+45A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+45A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+45A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5967
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4727
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

4-77018875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018875
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018875
    reference: chr 4
allele count: 1
allele frequency: 8.307165761185599e-6
allele num: 120378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+46G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1233G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+46G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+46G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+46G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+46G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+46G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3073G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1233G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+46G>A
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38512
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2286
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

4-77018876-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018876
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018876
    reference: chr 4
allele count: 165
allele frequency: 1.371183539149368e-3
allele num: 120334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+47T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+47T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1232T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+47T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+47T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+47T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3072T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+47T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+47T>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1232T>A
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 6.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 4.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

4-77018879-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77018879
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77018879
    reference: chr 4
allele count: 2
allele frequency: 1.664585934248856e-5
allele num: 120150
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-1229C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.814+50C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.70+50C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.930+50C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-3069C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-1229C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.232+50C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.111+50C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.814+50C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.814+50C>T
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2877
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

4-77020066-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020066
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020066
    reference: chr 4
allele count: 1
allele frequency: 8.476731372382808e-6
allele num: 117970
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.931-42C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-42C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.233-42C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.112-42C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.815-42C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.815-42C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.71-42C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.815-42C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-42C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1882C>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2079
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1882
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

4-77020069-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020069
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020069
    reference: chr 4
allele count: 1
allele frequency: 8.468978133098461e-6
allele num: 118078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-39A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1879A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.233-39A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.71-39A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.815-39A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.112-39A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.815-39A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.931-39A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-39A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.815-39A>T
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

4-77020070-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020070
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020070
    reference: chr 4
allele count: 22
allele frequency: 1.864090832062362e-4
allele num: 118020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1878G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.233-38G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.815-38G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-38G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-38G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.815-38G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.815-38G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.112-38G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.71-38G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.931-38G>T
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5890
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22399
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18996
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 938
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2174
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

4-77020080-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020080
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020080
    reference: chr 4
allele count: 3
allele frequency: 2.536225757908797e-5
allele num: 118286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.233-28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.71-28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1868A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.815-28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.815-28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.112-28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.815-28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.931-28A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-28A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19986
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 844
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2016
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

4-77020085-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020085
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020085
    reference: chr 4
allele count: 18
allele frequency: 1.519987840097279e-4
allele num: 118422
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-23A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1863A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.233-23A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.112-23A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.71-23A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.815-23A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.815-23A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-23A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.815-23A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.931-23A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27365
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20300
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

4-77020088-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020088
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020088
    reference: chr 4
allele count: 1
allele frequency: 8.437252155717926e-6
allele num: 118522
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-20A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.815-20A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.815-20A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.233-20A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.71-20A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.112-20A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.815-20A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-20A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.931-20A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1860A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6243
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46148
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum

4-77020093-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020093
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020093
    reference: chr 4
allele count: 3
allele frequency: 2.527081894300588e-5
allele num: 118714
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.71-15A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.815-15A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.112-15A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1855A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.233-15A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.931-15A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-15A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.815-15A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.815-15A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-15A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20827
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6088
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/4-77020097-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020097
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020097
    reference: chr 4
allele count: 2
allele frequency: 1.683246646131057e-5
allele num: 118818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.112-11C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.931-11C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.71-11C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-11C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.815-11C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-11C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.815-11C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.233-11C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1851C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.815-11C>A
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

4-77020099-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020099
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020099
    reference: chr 4
allele count: 1
allele frequency: 8.410287463625507e-6
allele num: 118902
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.71-9G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-9G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.931-9G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.112-9G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.233-9G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-9G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.815-9G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1849G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.815-9G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.815-9G>C
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48086
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/4-77020105-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020105
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020105
    reference: chr 4
allele count: 6
allele frequency: 5.040746030412501e-5
allele num: 119030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.112-3C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.815-3C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.931-3C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.233-3C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.38-3C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1843C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.815-3C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.79-3C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.71-3C>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.815-3C>A
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29249
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21538
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6305
  bin: 6.75e1
  variant carriers: 0
hgvs: c.815-3C>A
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD

4-77020138-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020138
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020138
    reference: chr 4
allele count: 1
allele frequency: 8.584427847883938e-6
allele num: 116490
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1810C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.845C>T
  hgvsp: ENSP00000343843.5:p.Pro282Leu
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.845C>T
  hgvsp: ENSP00000304313.5:p.Pro282Leu
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.263C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.101C>T
  hgvsp: ENSP00000422249.1:p.Pro34Leu
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.142C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.68C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.845C>T
  hgvsp: ENSP00000348064.4:p.Pro282Leu
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.109C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.961C>T
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21908
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro282Leu
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

4-77020145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020145
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020145
    reference: chr 4
allele count: 2
allele frequency: 1.745810055865922e-5
allele num: 114560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+5G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1803G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+5G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+5G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.968G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+5G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+5G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+5G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+5G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+5G>A
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
hgvs: c.847+5G>A
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

4-77020146-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020146
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020146
    reference: chr 4
allele count: 34
allele frequency: 2.983031813156925e-4
allele num: 113978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1802T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+6T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+6T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+6T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.969T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+6T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+6T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+6T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+6T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+6T>C
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23919
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21624
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
hgvs: c.847+6T>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

4-77020184-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020184
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020184
    reference: chr 4
allele count: 1
allele frequency: 1.254768118851636e-5
allele num: 79696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+44G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1007G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1764G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+44G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+44G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+44G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+44G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+44G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+44G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+44G>A
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8863
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18741
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2875
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

4-77020192-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020192
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020192
    reference: chr 4
allele count: 1
allele frequency: 1.386078230255316e-5
allele num: 72146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+52C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+52C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+52C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+52C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+52C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+52C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+52C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1756C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1015C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+52C>T
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21090
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2879
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

4-77020193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020193
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020193
    reference: chr 4
allele count: 3
allele frequency: 4.190295276140459e-5
allele num: 71594
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1755G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+53G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+53G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+53G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1016G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+53G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+53G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+53G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+53G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+53G>A
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21322
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17251
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1558
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31818
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

4-77020204-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020204
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020204
    reference: chr 4
allele count: 1
allele frequency: 1.577834579822651e-5
allele num: 63378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+64C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1027C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1744C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+64C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+64C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+64C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+64C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+64C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+64C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+64C>T
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16616
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5005
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

4-77020207-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020207
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020207
    reference: chr 4
allele count: 18
allele frequency: 2.962475312705728e-4
allele num: 60760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+67C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+67C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1030C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+67C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+67C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+67C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1741C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+67C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+67C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+67C>T
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24050
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 16273
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

4-77020208-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020208
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020208
    reference: chr 4
allele count: 30
allele frequency: 5.550210908014505e-4
allele num: 54052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+68G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+68G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1031G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+68G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+68G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1740G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+68G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+68G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+68G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+68G>A
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24287
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15821
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30879
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1432
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

4-77020208-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020208
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020208
    reference: chr 4
allele count: 1
allele frequency: 1.850070302671501e-5
allele num: 54052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+68G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+68G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+68G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+68G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+68G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+68G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1031G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1740G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+68G>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+68G>T
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15821
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1432
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

4-77020209-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020209
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020209
    reference: chr 4
allele count: 1
allele frequency: 1.770350175264667e-5
allele num: 56486
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+69C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+69C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+69C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+69C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+69C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1739C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1032C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+69C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+69C>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+69C>G
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15694
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1200
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

4-77020212-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020212
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020212
    reference: chr 4
allele count: 2
allele frequency: 3.653902367728734e-5
allele num: 54736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1736T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+72T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+72T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1035T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+72T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+72T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+72T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+72T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+72T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+72T>C
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15105
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24873
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2284
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

4-77020219-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020219
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020219
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 48018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+79C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+79C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+79C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+79C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+79C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1729C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+79C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+79C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+79C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1042C>T
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 9669
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25861
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31058
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

4-77020220-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020220
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020220
    reference: chr 4
allele count: 3
allele frequency: 6.593986284508528e-5
allele num: 45496
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1728C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1043C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+80C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+80C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+80C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+80C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+80C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+80C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+80C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+80C>T
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25934
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4336
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

4-77020221-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020221
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020221
    reference: chr 4
allele count: 32
allele frequency: 7.333058343645446e-4
allele num: 43638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+81G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1044G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+81G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+81G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+81G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+81G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+81G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1727G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+81G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+81G>A
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12226
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11096
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26019
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3034
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29348
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6341
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 7.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

4-77020224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020224
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020224
    reference: chr 4
allele count: 5
allele frequency: 1.149848220034955e-4
allele num: 43484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+84G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+84G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+84G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1724G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+84G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+84G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+84G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1047G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+84G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+84G>A
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26321
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11605
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11777
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6545
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

4-77020227-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020227
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020227
    reference: chr 4
allele count: 1
allele frequency: 2.54530645489717e-5
allele num: 39288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+87A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+87A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+87A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+87A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1721A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+87A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+87A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+87A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+87A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1050A>G
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26034
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12822
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

4-77020233-TCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020233
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020231
    reference: chr 4
allele count: 2
allele frequency: 5.345021112833396e-5
allele num: 37418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+95_144+96delAC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1058_1059delAC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+95_265+96delAC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+95_70+96delAC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+95_847+96delAC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+95_847+96delAC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1713_79-1712delAC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+95_103+96delAC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+95_847+96delAC
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+95_111+96delAC
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10043
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15373
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25394
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1298
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: TCA
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

4-77020271-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020271
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020271
    reference: chr 4
allele count: 1
allele frequency: 5.36135535063264e-5
allele num: 18652
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+131A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1677A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+131A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+131A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+131A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1094A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+131A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+131A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+131A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+131A>G
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12969
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

4-77020275-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020275
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020275
    reference: chr 4
allele count: 1
allele frequency: 6.3403499873193e-5
allele num: 15772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+135C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+135C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+135C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1098C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1673C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+135C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+135C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+135C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+135C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+135C>T
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

4-77020276-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020276
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020276
    reference: chr 4
allele count: 24
allele frequency: 1.516300227445034e-3
allele num: 15828
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+136G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+136G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+136G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1672G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1099G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+136G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+136G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+136G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+136G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+136G>A
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4960
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11404
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 32755
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33303
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 11308
  bin: 2.25e1
  variant carriers: 2
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

4-77020286-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020286
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020286
    reference: chr 4
allele count: 2
allele frequency: 1.676164934629568e-4
allele num: 11932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+146C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1109C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+146C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1662C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+146C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+146C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+146C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+146C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+146C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+146C>T
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32860
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

4-77020302-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020302
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020302
    reference: chr 4
allele count: 1
allele frequency: 1.428163381890888e-4
allele num: 7002
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+162A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+162A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1646A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+162A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+162A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+162A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1125A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+162A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+162A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+162A>G
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

4-77020305-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020305
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020305
    reference: chr 4
allele count: 2
allele frequency: 3.746721618583739e-4
allele num: 5338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+165C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+165C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+165C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+165C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+165C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1128C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+165C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1643C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+165C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+165C>T
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5167
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27182
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25528
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3511
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

4-77020312-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020312
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020312
    reference: chr 4
allele count: 1
allele frequency: 2.551020408163266e-4
allele num: 3920
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1636A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+172A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+172A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+172A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+172A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+172A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+172A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+172A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1135A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+172A>G
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25525
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

4-77020313-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020313
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020313
    reference: chr 4
allele count: 95
allele frequency: 2.32843137254902e-2
allele num: 4080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+173G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+173G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1635G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+173G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+173G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+173G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+173G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1136G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+173G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+173G>A
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25194
  bin: 2.5e0
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 7.5e0
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 1.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 2.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 6.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 9.75e1
  variant carriers: 113
num of homozygotes: 3
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

4-77020318-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020318
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020318
    reference: chr 4
allele count: 20
allele frequency: 6.199628022318661e-3
allele num: 3226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+178G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+178G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+178G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+178G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+178G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+178G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1630G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+178G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1141G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+178G>C
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24052
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 7.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22656
  bin: 7.5e0
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 3
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

4-77020342-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77020342
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77020342
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 1558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.70+202C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000513494
  gene symbol: ART3
  hgvsc: ENST00000513494.1:n.1165C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.144+202C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.847+202C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.265+202C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-1606C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.111+202C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.103+202C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.847+202C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.847+202C>T
  variant of: http://identifiers.org/hgnc/725
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1645
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16102
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

4-77021397-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77021397
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77021397
    reference: chr 4
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.145-47C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.266-47C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.848-47C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.112-47C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.104-47C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.848-47C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.71-47C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-551C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.848-47C>T
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11411
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2649
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

4-77021407-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77021407
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77021407
    reference: chr 4
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.71-37A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.848-37A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.848-37A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.848-37A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.266-37A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.104-37A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.112-37A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.145-37A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-541A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11411
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1396
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

4-77021410-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77021410
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77021410
    reference: chr 4
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.848-34G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-538G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.112-34G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.104-34G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.71-34G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.145-34G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.848-34G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.848-34G>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.266-34G>C
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11411
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

4-77021418-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77021418
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77021418
    reference: chr 4
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-530T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.848-26T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.848-26T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.266-26T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.848-26T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.104-26T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.145-26T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.71-26T>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.112-26T>C
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

4-77021420-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77021420
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77021420
    reference: chr 4
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.266-24A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.112-24A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.104-24A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.848-24A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.145-24A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.848-24A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.71-24A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.848-24A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-528A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

4-77021423-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77021423
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77021423
    reference: chr 4
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.145-21A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-525A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.71-21A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.266-21A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.112-21A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.848-21A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.848-21A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.104-21A>G
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.848-21A>G
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3200
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-77021424-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77021424
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77021424
    reference: chr 4
allele count: 90
allele frequency: 7.420477219134937e-4
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.848-20A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.848-20A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-524A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.145-20A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.266-20A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.112-20A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.848-20A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.104-20A>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.71-20A>T
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11439
  bin: 9.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

4-77021433-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77021433
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77021433
    reference: chr 4
allele count: 33322
allele frequency: 2.74625832399288e-1
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.848-11C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.848-11C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.266-11C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.145-11C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.71-11C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.848-11C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-515C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.112-11C>T
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.104-11C>T
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 5.75e1
  variant carriers: 410
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 5.25e1
  variant carriers: 416
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 2.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 2.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 3.25e1
  variant carriers: 161
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 9.25e1
  variant carriers: 866
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 7.75e1
  variant carriers: 537
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 7.25e1
  variant carriers: 474
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3252
  bin: 6.75e1
  variant carriers: 447
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 4.75e1
  variant carriers: 381
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 3.75e1
  variant carriers: 210
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 8.25e1
  variant carriers: 650
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 8.75e1
  variant carriers: 708
genotype depth: GenotypeDepth
  all individuals: 25099
  bin: 9.75e1
  variant carriers: 22204
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.25e1
  variant carriers: 331
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 6.25e1
  variant carriers: 416
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 7.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 8.25e1
  variant carriers: 11
num of homozygotes: 4864
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-77021442-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77021442
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77021442
    reference: chr 4
allele count: 17
allele frequency: 1.40185374542336e-4
allele num: 121268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.848-2A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.112-2A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.848-2A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.71-2A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.848-2A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.145-2A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.266-2A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-506A>C
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.104-2A>C
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4660
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
hgvs: c.848-2A>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

4-77021444-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 77021444
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 77021444
    reference: chr 4
allele count: 47
allele frequency: 3.875841139992084e-4
allele num: 121264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000504112
  gene symbol: ART3
  hgvsc: ENST00000504112.1:n.145G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000510669
  gene symbol: ART3
  hgvsc: ENST00000510669.1:n.266G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000343843
  ensembl transcript: ENST00000341029
  gene symbol: ART3
  hgvsc: ENST00000341029.5:c.848G>A
  hgvsp: ENSP00000343843.5:p.Gly283Asp
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506313
  gene symbol: ART3
  hgvsc: ENST00000506313.1:n.71G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000395688
  gene symbol: ART3
  hgvsc: ENST00000395688.3:n.79-504G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000348064
  ensembl transcript: ENST00000355810
  gene symbol: ART3
  hgvsc: ENST00000355810.4:c.848G>A
  hgvsp: ENSP00000348064.4:p.Gly283Asp
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl transcript: ENST00000506667
  gene symbol: ART3
  hgvsc: ENST00000506667.1:n.112G>A
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000304313
  ensembl transcript: ENST00000349321
  gene symbol: ART3
  hgvsc: ENST00000349321.3:c.848G>A
  hgvsp: ENSP00000304313.5:p.Gly283Asp
  variant of: http://identifiers.org/hgnc/725
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156219
  ensembl protein: ENSP00000422249
  ensembl transcript: ENST00000511188
  gene symbol: ART3
  hgvsc: ENST00000511188.1:c.104G>A
  hgvsp: ENSP00000422249.1:p.Gly35Asp
  variant of: http://identifiers.org/hgnc/725
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 9.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5246
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4648
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly283Asp
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1390
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 247
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2404
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38517
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 1561
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2721
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.141e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.959244e6

FS
type: SiteQuality
SIO_000300: 9.89e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.487e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.429999999999999e-1

QD
type: SiteQuality
SIO_000300: 7.92e0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2575
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2404
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38516
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8930
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1562
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2721
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1392
bin: 7.25e1
variant carriers: 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: 6610
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: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.105e1

MQ
type: SiteQuality
SIO_000300: 5.815e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.61e-1

DP
type: SiteQuality
SIO_000300: 2.959307e6

VQSLOD
type: SiteQuality
SIO_000300: -2.968e0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2579
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2722
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1392
bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

South Asian
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allele frequency: 1.221299462628236e-4
allele num: 16376
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

ClippingRankSum
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SIO_000300: 3.98e-1

FS
type: SiteQuality
SIO_000300: 7.0e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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MQRankSum
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SIO_000300: 2.28e0

DP
type: SiteQuality
SIO_000300: 2.958919e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.85e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
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: 900
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.64e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

VQSLOD
type: SiteQuality
SIO_000300: 1.53e-1

QD
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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SIO_000300: -8.53e-1

DP
type: SiteQuality
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BaseQRankSum
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SIO_000300: -3.844e0

FS
type: SiteQuality
SIO_000300: 1.664e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.05e-1

GenotypeQuality
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variant carriers: 0

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

Latino
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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: 8652
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: 66610
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.113964294448521e-5
allele num: 16356
num of homozygotes: 0

QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.957399e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.25e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16352
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: 0
allele frequency: 0.0e0
allele num: 66606
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.947533896639811e-4
allele num: 10178
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
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.957e0

QD
type: SiteQuality
SIO_000300: 1.495e1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.161e0

InbreedingCoeff
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SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.12e-1

DP
type: SiteQuality
SIO_000300: 2.956587e6

FS
type: SiteQuality
SIO_000300: 5.082e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.223540927444023e-4
allele num: 16346
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-2

DP
type: SiteQuality
SIO_000300: 2.956302e6

BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 7.42e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.065e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 3.145e0

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501907422426482e-5
allele num: 66582
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.968503937007874e-4
allele num: 10160
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16316
num of homozygotes: 0

European (Finnish)
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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: 902
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.954373e6

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.281e1

MQ
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
SIO_000300: 7.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
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South Asian
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allele count: 1
allele frequency: 6.140243153628883e-5
allele num: 16286
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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QD
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MQ
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
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allele num: 66562
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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Other
type: Population
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Latino
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allele num: 11564
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South Asian
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QD
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

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

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

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

South Asian
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allele frequency: 6.150818058801821e-5
allele num: 16258
num of homozygotes: 0

QD
type: SiteQuality
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FS
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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MQ
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10078
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502629601803156e-5
allele num: 66550
num of homozygotes: 0

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

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

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

ClippingRankSum
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SIO_000300: -9.13e-1

BaseQRankSum
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FS
type: SiteQuality
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MQ
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.4e-3

ReadPosRankSum
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MQRankSum
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DP
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SIO_000300: 2.940222e6

QD
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SIO_000300: 1.381e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502584445245823e-5
allele num: 66552
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.059e1

BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.492e0

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10078
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.171315724512466e-5
allele num: 16204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66518
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.401e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.129e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: 6.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

DP
type: SiteQuality
SIO_000300: 2.934273e6

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

East Asian
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allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10076
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.022e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.233e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.503804625703029e-5
allele num: 66498
num of homozygotes: 0

Other
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South Asian
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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FS
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QD
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ClippingRankSum
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VQSLOD
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DP
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele count: 19
allele frequency: 2.197039777983349e-3
allele num: 8648
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66492
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Latino
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African
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allele count: 0
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BaseQRankSum
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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FS
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 7.068519521145401e-4
allele num: 66492
num of homozygotes: 1

African
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European (Finnish)
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Other
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South Asian
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East Asian
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Latino
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allele frequency: 6.055363321799307e-4
allele num: 11560
num of homozygotes: 0

MQRankSum
type: SiteQuality
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DP
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FS
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 0
allele frequency: 0.0e0
allele num: 66474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10056
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: 16134
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.820000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.97e-1

FS
type: SiteQuality
SIO_000300: 3.067e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

QD
type: SiteQuality
SIO_000300: 1.313e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.871e0

DP
type: SiteQuality
SIO_000300: 2.930559e6

GenotypeQuality
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 165

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3993
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 395
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008785654110001e-5
allele num: 66472
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.055363321799307e-4
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 156
allele frequency: 1.552238805970149e-2
allele num: 10050
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: 16094
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 8.159999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

QD
type: SiteQuality
SIO_000300: 1.371e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.237e0

MQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

DP
type: SiteQuality
SIO_000300: 2.931444e6

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

GenotypeQuality
all individuals: 2126
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2393
bin: 8.25e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.116071428571429e-3
allele num: 896
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66424
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: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.248437890527369e-5
allele num: 16004
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.217e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

DP
type: SiteQuality
SIO_000300: 2.931452e6

FS
type: SiteQuality
SIO_000300: 1.611e0

VQSLOD
type: SiteQuality
SIO_000300: 6.02e-1

QD
type: SiteQuality
SIO_000300: 1.131e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.837e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539882968894364e-5
allele num: 64940
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.67e-1

QD
type: SiteQuality
SIO_000300: 7.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.804999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.387839e6

GenotypeQuality
all individuals: 2771
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

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

GenotypeQuality
all individuals: 6061
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variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64982
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15588
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.828975820719482e-5
allele num: 10174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.71e-1

QD
type: SiteQuality
SIO_000300: 1.018e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.873e1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.22e-2

FS
type: SiteQuality
SIO_000300: 2.546e0

DP
type: SiteQuality
SIO_000300: 1.397232e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.12e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 288
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15586
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

East Asian
type: Population
allele count: 22
allele frequency: 2.575509248419574e-3
allele num: 8542
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.05e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

DP
type: SiteQuality
SIO_000300: 1.400574e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.187e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.401e0

GenotypeQuality
all individuals: 77
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15690
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.640845070422535e-4
allele num: 11360
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.43631e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

QD
type: SiteQuality
SIO_000300: 8.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.04e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.638e0

VQSLOD
type: SiteQuality
SIO_000300: 1.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 18

GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

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

South Asian
type: Population
allele count: 18
allele frequency: 1.143292682926829e-3
allele num: 15744
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65130
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

FS
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.281e1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.450892e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 826
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534542552864991e-5
allele num: 65166
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

South Asian
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allele count: 0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

DP
type: SiteQuality
SIO_000300: 1.458981e6

VQSLOD
type: SiteQuality
SIO_000300: 7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 4.749e0

QD
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SIO_000300: 1.356e1

ClippingRankSum
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SIO_000300: -1.218e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 15894
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.597560228038987e-5
allele num: 65252
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -1.189e0

ClippingRankSum
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.943e1

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.063725490196078e-5
allele num: 65280
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.83e-1

DP
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MQ
type: SiteQuality
SIO_000300: 5.818e1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -4.658e-1

BaseQRankSum
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SIO_000300: -1.686e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

QD
type: SiteQuality
SIO_000300: 1.06e1

ReadPosRankSum
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SIO_000300: -5.6e-2

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531534291052777e-5
allele num: 65294
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

FS
type: SiteQuality
SIO_000300: 2.073e0

MQRankSum
type: SiteQuality
SIO_000300: 7.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.08e-1

QD
type: SiteQuality
SIO_000300: 1.504e1

DP
type: SiteQuality
SIO_000300: 1.482142e6

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.336994624912363e-4
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65328
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.482929857231533e-4
allele num: 16110
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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BaseQRankSum
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MQ
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SIO_000300: 5.982e1

DP
type: SiteQuality
SIO_000300: 1.48947e6

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.87e-1

InbreedingCoeff
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SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.101e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.568676664365941e-5
allele num: 63748
num of homozygotes: 0

Other
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South Asian
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allele frequency: 0.0e0
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VQSLOD
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BaseQRankSum
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MQ
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FS
type: SiteQuality
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DP
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 62582
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South Asian
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African
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East Asian
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FS
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
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ReadPosRankSum
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ClippingRankSum
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MQ
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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Latino
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allele frequency: 5.449591280653951e-4
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European (Non-Finnish)
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allele frequency: 4.499726802301289e-4
allele num: 62226
num of homozygotes: 0

South Asian
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East Asian
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Other
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BaseQRankSum
type: SiteQuality
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MQ
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InbreedingCoeff
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QD
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FS
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DP
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MQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele num: 650
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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Latino
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South Asian
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allele frequency: 7.978299026647519e-5
allele num: 12534
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 42588
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

VQSLOD
type: SiteQuality
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DP
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BaseQRankSum
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SIO_000300: -2.275e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
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SIO_000300: 8.67e0

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3852
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 11928
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
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African
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4874
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6232
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.618623651408819e-5
allele num: 38188
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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MQ
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SIO_000300: 5.247e1

QD
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

FS
type: SiteQuality
SIO_000300: 9.779e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.28e-1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11884
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 37850
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3826
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African
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allele count: 2
allele frequency: 3.121098626716604e-4
allele num: 6408
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.666666666666667e-3
allele num: 600
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.595e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-2

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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FS
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -9.19e-1

QD
type: SiteQuality
SIO_000300: 7.61e0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 5316
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.461841457410143e-4
allele num: 4062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3370
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 33290
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11212
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
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MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.127e0

DP
type: SiteQuality
SIO_000300: 7.65173e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.36e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.589e0

QD
type: SiteQuality
SIO_000300: 2.909e1

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

South Asian
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allele count: 1
allele frequency: 9.167583425009168e-5
allele num: 10908
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.29009938357026e-5
allele num: 31796
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.982553528945282e-4
allele num: 5044
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 1.297738227660363e-3
allele num: 5394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 2.180685358255452e-3
allele num: 3210
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

FS
type: SiteQuality
SIO_000300: 3.021e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.56e-2

DP
type: SiteQuality
SIO_000300: 7.47857e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

QD
type: SiteQuality
SIO_000300: 1.357e1

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

East Asian
type: Population
allele count: 1
allele frequency: 2.910360884749709e-4
allele num: 3436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

European (Non-Finnish)
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allele count: 25
allele frequency: 9.00446621524276e-4
allele num: 27764
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 474
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European (Finnish)
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allele count: 2
allele frequency: 6.788866259334691e-4
allele num: 2946
num of homozygotes: 0

African
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allele count: 2
allele frequency: 4.006410256410256e-4
allele num: 4992
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VQSLOD
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SIO_000300: -1.711e0

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4164
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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allele num: 10276
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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QD
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ReadPosRankSum
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
type: Population
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Other
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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MQ
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BaseQRankSum
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FS
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.049203440011279e-5
allele num: 28372
num of homozygotes: 0

South Asian
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European (Finnish)
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allele frequency: 0.0e0
allele num: 2882
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African
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Latino
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allele frequency: 0.0e0
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East Asian
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Other
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FS
type: SiteQuality
SIO_000300: 2.1e0

BaseQRankSum
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SIO_000300: -5.99e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.797e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.055e0

MQ
type: SiteQuality
SIO_000300: 5.777e1

DP
type: SiteQuality
SIO_000300: 7.03612e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.93e-2

QD
type: SiteQuality
SIO_000300: 1.239e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3494
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

DP
type: SiteQuality
SIO_000300: 6.57779e5

VQSLOD
type: SiteQuality
SIO_000300: -1.998e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.21e-2

QD
type: SiteQuality
SIO_000300: 5.23e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 267
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 8.643042350907519e-5
allele num: 23140
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.056635672020287e-4
allele num: 9464
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3194
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2420
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

FS
type: SiteQuality
SIO_000300: 4.337e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.73e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.4915e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

QD
type: SiteQuality
SIO_000300: 8.6e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 248
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 30

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 2

African
type: Population
allele count: 30
allele frequency: 7.2992700729927e-3
allele num: 4110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2320
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9320
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 6.729475100942127e-4
allele num: 2972
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.63e0

QD
type: SiteQuality
SIO_000300: 1.376e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.86e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.33159e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.926e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 4.359197907585005e-4
allele num: 2294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.81257930034439e-4
allele num: 22068
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4044
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2978
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.402e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.86e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.56e-2

DP
type: SiteQuality
SIO_000300: 6.23111e5

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 865
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2084
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3758
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.070479667376534e-5
allele num: 19722
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.52e-2

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -3.206e0

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -2.18e0

QD
type: SiteQuality
SIO_000300: 7.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.3e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 6.06494e5

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3548
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1956
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 18724
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 2254
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1878
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 2.292000916800367e-4
allele num: 8726
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-2

DP
type: SiteQuality
SIO_000300: 5.70155e5

BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 2.044e1

MQ
type: SiteQuality
SIO_000300: 5.705e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.965243296921549e-4
allele num: 2014
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.03e1

DP
type: SiteQuality
SIO_000300: 3.38708e5

QD
type: SiteQuality
SIO_000300: 4.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.78e-2

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.86e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.594e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 14
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 69
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.007226013649137e-4
allele num: 4982
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7416
num of homozygotes: 0

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

MQ
type: SiteQuality
SIO_000300: 5.685e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.630000000000001e-2

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.6e-2

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 68
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1005
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1062
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1658
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 562
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 9.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 4.640371229698376e-3
allele num: 5172
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1694
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7352
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.33e-2

DP
type: SiteQuality
SIO_000300: 3.05149e5

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

QD
type: SiteQuality
SIO_000300: 1.408e1

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8222
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2032
bin: 2.5e0
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GenotypeQuality
all individuals: 32786
bin: 7.5e0
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GenotypeQuality
all individuals: 62
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 4.699248120300752e-4
allele num: 4256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5316
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.04e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.809e0

VQSLOD
type: SiteQuality
SIO_000300: -5.528e-1

DP
type: SiteQuality
SIO_000300: 2.42894e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQ
type: SiteQuality
SIO_000300: 5.732e1

QD
type: SiteQuality
SIO_000300: 6.38e0

GenotypeQuality
all individuals: 29
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27315
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4984
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2398
bin: 2.5e0
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GenotypeQuality
all individuals: 348
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 681
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.229974160206718e-4
allele num: 3096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.682e1

MQRankSum
type: SiteQuality
SIO_000300: 6.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.790000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.36e-1

DP
type: SiteQuality
SIO_000300: 1.66951e5

QD
type: SiteQuality
SIO_000300: 9.77e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.0e-2

GenotypeQuality
all individuals: 501
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4163
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 97
bin: 6.75e1
variant carriers: 1

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

African
type: Population
allele count: 2
allele frequency: 2.890173410404624e-3
allele num: 692
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.55e-2

MQ
type: SiteQuality
SIO_000300: 5.919e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.533e0

QD
type: SiteQuality
SIO_000300: 1.377e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

DP
type: SiteQuality
SIO_000300: 1.5449e5

GenotypeQuality
all individuals: 554
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24012
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2772
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3530
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 956
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1936
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.731343283582089e-3
allele num: 268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.30088e5

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.865e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.470000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

QD
type: SiteQuality
SIO_000300: 8.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 23532
bin: 7.5e0
variant carriers: 41

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 15

GenotypeQuality
all individuals: 565
bin: 1.25e1
variant carriers: 11

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 587
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 12
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2474
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 3551
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 22
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 9
bin: 9.25e1
variant carriers: 9

GenotypeQuality
all individuals: 400
bin: 6.25e1
variant carriers: 14

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 8

South Asian
type: Population
allele count: 2
allele frequency: 1.968503937007874e-3
allele num: 1016
num of homozygotes: 0

East Asian
type: Population
allele count: 24
allele frequency: 8.391608391608392e-2
allele num: 286
num of homozygotes: 1

African
type: Population
allele count: 63
allele frequency: 1.060606060606061e-1
allele num: 594
num of homozygotes: 2

Latino
type: Population
allele count: 2
allele frequency: 1.515151515151515e-2
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 2.0e-3
allele num: 2000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 1.26509e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.389999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.596e1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
all individuals: 510
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 183
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 57
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3092
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 351
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 142
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 12
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 23
bin: 9.75e1
variant carriers: 23

African
type: Population
allele count: 19
allele frequency: 3.682170542635659e-2
allele num: 516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.510574018126888e-3
allele num: 662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1658
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.130000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

FS
type: SiteQuality
SIO_000300: 1.264e0

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 1.12562e5

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.167e1

GenotypeQuality
all individuals: 289
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1727
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 80
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.75e1
variant carriers: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.897e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.61e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

DP
type: SiteQuality
SIO_000300: 6.7642e4

QD
type: SiteQuality
SIO_000300: 1.092e1

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 74
bin: 2.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e-1

QD
type: SiteQuality
SIO_000300: 1.371e1

MQ
type: SiteQuality
SIO_000300: 5.896e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.222e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -9.429999999999999e-2

DP
type: SiteQuality
SIO_000300: 4.492963e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

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

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.686168151879117e-5
allele num: 10324
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.104e1

FS
type: SiteQuality
SIO_000300: 4.319e0

MQRankSum
type: SiteQuality
SIO_000300: 9.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.347e-1

InbreedingCoeff
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.92e-1

DP
type: SiteQuality
SIO_000300: 4.495279e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.519e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.347e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 51669
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.495847e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 9.96e-1

QD
type: SiteQuality
SIO_000300: 1.313e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

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

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

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: 11574
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 4.497128e6

QD
type: SiteQuality
SIO_000300: 9.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.85e-1

MQ
type: SiteQuality
SIO_000300: 5.893e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 606
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GenotypeQuality
all individuals: 51672
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 905
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3185
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-2

MQ
type: SiteQuality
SIO_000300: 5.944e1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

DP
type: SiteQuality
SIO_000300: 4.497277e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.433e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e0

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

GenotypeQuality
all individuals: 50
bin: 3.25e1
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GenotypeQuality
all individuals: 905
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 51672
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 738
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variant carriers: 0

GenotypeQuality
all individuals: 900
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 1418
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
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: 66720
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 4.497486e6

FS
type: SiteQuality
SIO_000300: 9.260999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: -6.24e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 20
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3205
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51678
bin: 9.75e1
variant carriers: 90

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.456022118541559e-4
allele num: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 86
allele frequency: 8.336564559906941e-3
allele num: 10316
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.17e0

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.333e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.28e-1

DP
type: SiteQuality
SIO_000300: 4.500942e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.844e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.15e-1

QD
type: SiteQuality
SIO_000300: 1.543e1

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 2

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

GenotypeQuality
all individuals: 9
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variant carriers: 5

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 2645
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variant carriers: 7

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 53801
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variant carriers: 28380

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1125
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GenotypeQuality
all individuals: 651
bin: 9.25e1
variant carriers: 11

GenotypeQuality
all individuals: 528
bin: 7.25e1
variant carriers: 4

South Asian
type: Population
allele count: 2887
allele frequency: 1.748637189582072e-1
allele num: 16510
num of homozygotes: 263

European (Non-Finnish)
type: Population
allele count: 18161
allele frequency: 2.721564513711974e-1
allele num: 66730
num of homozygotes: 2486

East Asian
type: Population
allele count: 3247
allele frequency: 3.752022186272244e-1
allele num: 8654
num of homozygotes: 620

African
type: Population
allele count: 4295
allele frequency: 4.1505604947816e-1
allele num: 10348
num of homozygotes: 892

European (Finnish)
type: Population
allele count: 1762
allele frequency: 2.664851784633999e-1
allele num: 6612
num of homozygotes: 229

Other
type: Population
allele count: 238
allele frequency: 2.621145374449339e-1
allele num: 908
num of homozygotes: 38

Latino
type: Population
allele count: 2732
allele frequency: 2.360463106963885e-1
allele num: 11574
num of homozygotes: 336

QD
type: SiteQuality
SIO_000300: 1.645e1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

DP
type: SiteQuality
SIO_000300: 5.814671e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

FS
type: SiteQuality
SIO_000300: 5.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.627e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.59e-1

GenotypeQuality
all individuals: 4636
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 48197
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variant carriers: 17

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 798
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 940
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GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 2034
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GenotypeQuality
all individuals: 1290
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 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 (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

African
type: Population
allele count: 17
allele frequency: 1.652731868559207e-3
allele num: 10286
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

QD
type: SiteQuality
SIO_000300: 1.218e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.93e-1

MQ
type: SiteQuality
SIO_000300: 5.752e1

DP
type: SiteQuality
SIO_000300: 3.808364e6

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-1

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

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

GenotypeQuality
all individuals: 2030
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0