2-63215137-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63215137
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63215137
    reference: chr 2
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-2714G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-2714G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2785G>A
  hgvsp: ENSP00000263991.5:p.Glu929Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2680G>A
  hgvsp: ENSP00000346482.3:p.Glu894Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-2714G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2680G>A
  hgvsp: ENSP00000385524.1:p.Glu894Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.263G>A
  hgvsp: ENSP00000388442.1:p.Glu89Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000399927
  ensembl transcript: ENST00000444311
  gene symbol: EHBP1
  hgvsc: ENST00000444311.1:c.458G>A
  hgvsp: ENSP00000399927.1:p.Glu154Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-2714G>A
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4266
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu929Lys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum

2-63215142-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63215142
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63215142
    reference: chr 2
allele count: 3
allele frequency: 2.474267616785431e-5
allele num: 121248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-2709T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-2709T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-2709T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2685T>C
  hgvsp: ENST00000405289.1:c.2685T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2790T>C
  hgvsp: ENST00000263991.5:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2685T>C
  hgvsp: ENST00000354487.3:c.2685T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.268T>C
  hgvsp: ENST00000422032.1:c.268T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-2709T>C
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4268
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu930Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

2-63215167-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63215167
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63215167
    reference: chr 2
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2815A>T
  hgvsp: ENSP00000263991.5:p.Thr939Ser
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2710A>T
  hgvsp: ENSP00000346482.3:p.Thr904Ser
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2710A>T
  hgvsp: ENSP00000385524.1:p.Thr904Ser
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.293A>T
  hgvsp: ENSP00000388442.1:p.Thr99Ser
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-2684A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-2684A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-2684A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-2684A>T
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6839
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr939Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

2-63215173-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63215173
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63215173
    reference: chr 2
allele count: 1
allele frequency: 8.257501940512956e-6
allele num: 121102
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2716G>A
  hgvsp: ENSP00000385524.1:p.Glu906Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2716G>A
  hgvsp: ENSP00000346482.3:p.Glu906Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-2678G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.299G>A
  hgvsp: ENSP00000388442.1:p.Glu101Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2821G>A
  hgvsp: ENSP00000263991.5:p.Glu941Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-2678G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-2678G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-2678G>A
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4267
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40662
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1850
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu941Lys
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

2-63215177-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63215177
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63215177
    reference: chr 2
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-2674A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2821+4A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-2674A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.299+4A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2716+4A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-2674A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-2674A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2716+4A>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40577
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
hgvs: c.2821+4A>G
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

2-63215183-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63215183
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63215183
    reference: chr 2
allele count: 1
allele frequency: 8.265965712774223e-6
allele num: 120978
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2821+10A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2716+10A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-2668A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2716+10A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-2668A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-2668A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.299+10A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-2668A>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10779
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2086
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2727
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4267
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

2-63215195-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63215195
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63215195
    reference: chr 2
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2821+22T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-2656T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-2656T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-2656T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2716+22T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.299+22T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2716+22T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-2656T>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1843
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

2-63215196-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63215196
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63215196
    reference: chr 2
allele count: 1
allele frequency: 8.283219853221344e-6
allele num: 120726
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-2655T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2716+23T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.299+23T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-2655T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2716+23T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2821+23T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-2655T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-2655T>A
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4268
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6768
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

2-63215198-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63215198
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63215198
    reference: chr 2
allele count: 35
allele frequency: 2.901482242928673e-4
allele num: 120628
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2716+25G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.299+25G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-2653G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2716+25G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2821+25G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-2653G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-2653G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-2653G>A
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 37925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10685
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2710
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

2-63215198-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63215198
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63215198
    reference: chr 2
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.299+25G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2716+25G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-2653G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2716+25G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-2653G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2821+25G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-2653G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-2653G>T
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39242
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2710
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum

2-63215208-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63215208
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63215208
    reference: chr 2
allele count: 1
allele frequency: 8.313381218409152e-6
allele num: 120288
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2821+35G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2716+35G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-2643G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-2643G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.299+35G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-2643G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2716+35G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-2643G>A
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35845
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37199
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1732
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

http://identifiers.org/exac.variant/2-63215216-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63215216
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63215216
    reference: chr 2
allele count: 2
allele frequency: 1.66741700431861e-5
allele num: 119946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-2635A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.299+43A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2716+43A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-2635A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2821+43A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-2635A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-2635A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2716+43A>C
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5188
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31953
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2157
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2044
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6425
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

2-63217800-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217800
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217800
    reference: chr 2
allele count: 1
allele frequency: 8.296138976920141e-6
allele num: 120538
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2822-51A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-51A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-51A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2717-51A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.300-51A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-51A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2717-51A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-51A>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4903
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18758
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

2-63217809-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217809
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217809
    reference: chr 2
allele count: 1
allele frequency: 8.294349888855711e-6
allele num: 120564
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-42T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-42T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.300-42T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-42T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-42T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2822-42T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2717-42T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2717-42T>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18743
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4662
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3128
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-63217820-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217820
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217820
    reference: chr 2
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-31C>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2717-31C>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2717-31C>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.300-31C>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-31C>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-31C>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2822-31C>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-31C>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2323
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

2-63217820-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217820
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217820
    reference: chr 2
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2717-31C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-31C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2717-31C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2822-31C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.300-31C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-31C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-31C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-31C>T
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14382
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2323
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18737
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

2-63217832-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217832
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217832
    reference: chr 2
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-19G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2717-19G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-19G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2822-19G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.300-19G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-19G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2717-19G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-19G>T
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6602
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4865
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4646
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15142
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6850
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

2-63217833-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217833
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217833
    reference: chr 2
allele count: 1
allele frequency: 8.279516476237788e-6
allele num: 120780
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2822-18T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.300-18T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2717-18T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2717-18T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-18T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-18T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-18T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-18T>C
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9057
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18738
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3121
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

2-63217840-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217840
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217840
    reference: chr 2
allele count: 8
allele frequency: 6.618243187345919e-5
allele num: 120878
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2822-11A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.300-11A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.225-11A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2717-11A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2609-11A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2717-11A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2609-11A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.14-11A>T
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9052
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11965
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3814
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6899
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4652
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

2-63217857-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217857
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217857
    reference: chr 2
allele count: 1
allele frequency: 8.263097008758882e-6
allele num: 121020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.231A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2828A>T
  hgvsp: ENSP00000263991.5:p.Asn943Ile
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2723A>T
  hgvsp: ENSP00000385524.1:p.Asn908Ile
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.306A>T
  hgvsp: ENSP00000388442.1:p.Asn103Ile
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2615A>T
  hgvsp: ENSP00000403783.1:p.Asn872Ile
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.20A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2615A>T
  hgvsp: ENSP00000384143.3:p.Asn872Ile
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2723A>T
  hgvsp: ENSP00000346482.3:p.Asn908Ile
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15718
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6919
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4865
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn943Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

2-63217871-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217871
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217871
    reference: chr 2
allele count: 1
allele frequency: 8.259957378619926e-6
allele num: 121066
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2842G>T
  hgvsp: ENSP00000263991.5:p.Asp948Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2737G>T
  hgvsp: ENSP00000346482.3:p.Asp913Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2629G>T
  hgvsp: ENSP00000403783.1:p.Asp877Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2737G>T
  hgvsp: ENSP00000385524.1:p.Asp913Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.245G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.34G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.320G>T
  hgvsp: ENSP00000388442.1:p.Asp108Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2629G>T
  hgvsp: ENSP00000384143.3:p.Asp877Tyr
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2324
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6929
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp948Tyr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

2-63217874-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217874
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217874
    reference: chr 2
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2845T>C
  hgvsp: ENST00000263991.5:c.2845T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.323T>C
  hgvsp: ENST00000422032.1:c.323T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2740T>C
  hgvsp: ENST00000354487.3:c.2740T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.37T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2740T>C
  hgvsp: ENST00000405289.1:c.2740T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2632T>C
  hgvsp: ENST00000405015.3:c.2632T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.248T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2632T>C
  hgvsp: ENST00000431489.1:c.2632T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3807
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4656
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15829
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu949Leu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS

2-63217894-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217894
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217894
    reference: chr 2
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.343A>G
  hgvsp: ENST00000422032.1:c.343A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.268A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2652A>G
  hgvsp: ENST00000431489.1:c.2652A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2865A>G
  hgvsp: ENST00000263991.5:c.2865A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2760A>G
  hgvsp: ENST00000354487.3:c.2760A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2760A>G
  hgvsp: ENST00000405289.1:c.2760A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2652A>G
  hgvsp: ENST00000405015.3:c.2652A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.57A>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3805
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18728
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu955Leu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-63217923-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217923
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217923
    reference: chr 2
allele count: 2
allele frequency: 1.650737054094653e-5
allele num: 121158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2789C>A
  hgvsp: ENSP00000346482.3:p.Pro930His
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.86C>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2681C>A
  hgvsp: ENSP00000403783.1:p.Pro894His
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.372C>A
  hgvsp: ENSP00000388442.1:p.Pro125His
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2681C>A
  hgvsp: ENSP00000384143.3:p.Pro894His
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2789C>A
  hgvsp: ENSP00000385524.1:p.Pro930His
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.297C>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2894C>A
  hgvsp: ENSP00000263991.5:p.Pro965His
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6942
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4647
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro965His
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

2-63217931-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217931
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217931
    reference: chr 2
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.305G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.94G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.380G>A
  hgvsp: ENSP00000388442.1:p.Ala128Thr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2902G>A
  hgvsp: ENSP00000263991.5:p.Ala968Thr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2797G>A
  hgvsp: ENSP00000385524.1:p.Ala933Thr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2797G>A
  hgvsp: ENSP00000346482.3:p.Ala933Thr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2689G>A
  hgvsp: ENSP00000384143.3:p.Ala897Thr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2689G>A
  hgvsp: ENSP00000403783.1:p.Ala897Thr
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2320
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala968Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

2-63217967-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217967
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217967
    reference: chr 2
allele count: 2
allele frequency: 1.652046059044126e-5
allele num: 121062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2725G>T
  hgvsp: ENSP00000403783.1:p.Asp909Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.416G>T
  hgvsp: ENSP00000388442.1:p.Asp140Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.130G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.341G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2938G>T
  hgvsp: ENSP00000263991.5:p.Asp980Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2833G>T
  hgvsp: ENSP00000385524.1:p.Asp945Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2833G>T
  hgvsp: ENSP00000346482.3:p.Asp945Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2725G>T
  hgvsp: ENSP00000384143.3:p.Asp909Tyr
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9030
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6596
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18722
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6930
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4866
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp980Tyr
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/2-63217970-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217970
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217970
    reference: chr 2
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.419A>C
  hgvsp: ENSP00000388442.1:p.Met141Leu
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2836A>C
  hgvsp: ENSP00000385524.1:p.Met946Leu
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.133A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2941A>C
  hgvsp: ENSP00000263991.5:p.Met981Leu
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2728A>C
  hgvsp: ENSP00000384143.3:p.Met910Leu
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.344A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2836A>C
  hgvsp: ENSP00000346482.3:p.Met946Leu
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2728A>C
  hgvsp: ENSP00000403783.1:p.Met910Leu
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15818
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met981Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-63217981-TCTTA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217981
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217977
    reference: chr 2
allele count: 10
allele frequency: 8.269930532583527e-5
allele num: 120920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.138+10_138+13delACTT
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2733+10_2733+13delACTT
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.424+10_424+13delACTT
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2841+10_2841+13delACTT
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.349+10_349+13delACTT
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2841+10_2841+13delACTT
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2946+10_2946+13delACTT
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2733+10_2733+13delACTT
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11963
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3127
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4637
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4858
  bin: 7.75e1
  variant carriers: 0
hgvs: c.2946+10_2946+13delACTT
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: TCTTA
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff

2-63217987-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217987
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217987
    reference: chr 2
allele count: 1
allele frequency: 8.273625337150233e-6
allele num: 120866
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2841+12T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.138+12T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.349+12T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2733+12T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2946+12T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2733+12T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.424+12T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2841+12T>C
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15196
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2320
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4848
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18721
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6846
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

2-63217987-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217987
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217987
    reference: chr 2
allele count: 16
allele frequency: 1.323780053944037e-4
allele num: 120866
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.424+12T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.349+12T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2841+12T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2946+12T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.138+12T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2733+12T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2733+12T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2841+12T>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9005
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6594
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13285
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4848
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4623
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2320
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

2-63217988-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63217988
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63217988
    reference: chr 2
allele count: 4
allele frequency: 3.309723969020984e-5
allele num: 120856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.424+13T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.138+13T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.349+13T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2733+13T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2946+13T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2841+13T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2841+13T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2733+13T>C
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6594
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3117
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18710
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 6848
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

2-63218003-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63218003
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63218003
    reference: chr 2
allele count: 4
allele frequency: 3.315924728508663e-5
allele num: 120630
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2946+28G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.349+28G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.138+28G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2841+28G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2733+28G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2733+28G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.424+28G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2841+28G>A
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6581
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11596
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8961
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18698
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4595
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD

2-63218004-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63218004
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63218004
    reference: chr 2
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.138+29C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2733+29C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.349+29C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2946+29C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2841+29C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2733+29C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.424+29C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2841+29C>T
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8952
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2303
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3036
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

2-63218005-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63218005
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63218005
    reference: chr 2
allele count: 2
allele frequency: 1.657742486282181e-5
allele num: 120646
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2946+30T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2841+30T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.424+30T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.349+30T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2733+30T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2733+30T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.138+30T>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2841+30T>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12828
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3785
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6530
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

2-63218009-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63218009
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63218009
    reference: chr 2
allele count: 1
allele frequency: 8.295450774795103e-6
allele num: 120548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2733+34T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2841+34T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2946+34T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.138+34T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2733+34T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2841+34T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.424+34T>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.349+34T>A
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3782
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4747
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4575
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/2-63218010-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63218010
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63218010
    reference: chr 2
allele count: 1
allele frequency: 8.290361625574107e-6
allele num: 120622
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2841+35A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.138+35A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2841+35A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2946+35A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.349+35A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.424+35A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2733+35A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2733+35A>C
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5493
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3020
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18689
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3780
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4756
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

2-63218014-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63218014
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63218014
    reference: chr 2
allele count: 1
allele frequency: 8.301786544464368e-6
allele num: 120456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.138+39G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2841+39G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.424+39G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2733+39G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2841+39G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2946+39G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2733+39G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.349+39G>A
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3771
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10643
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

2-63218025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63218025
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63218025
    reference: chr 2
allele count: 3
allele frequency: 2.495175993080045e-5
allele num: 120232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2733+50T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.138+50T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2946+50T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.424+50T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2733+50T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2841+50T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.349+50T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2841+50T>C
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9632
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8808
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3769
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1210
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

2-63220618-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220618
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220618
    reference: chr 2
allele count: 1
allele frequency: 8.636026046254556e-6
allele num: 115794
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.139-47T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2842-47T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2842-47T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2947-47T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.425-47T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2734-47T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.350-47T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2734-47T>C
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22999
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2032
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

2-63220623-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220623
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220623
    reference: chr 2
allele count: 2
allele frequency: 1.72666839333506e-5
allele num: 115830
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2734-42A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.139-42A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2947-42A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.350-42A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2734-42A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2842-42A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.425-42A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2842-42A>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23198
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14368
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1596
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1031
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1914
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

2-63220627-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220627
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220627
    reference: chr 2
allele count: 1
allele frequency: 8.624555835374478e-6
allele num: 115948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2842-38G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.425-38G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2947-38G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2842-38G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.350-38G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.139-38G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2734-38G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2734-38G>A
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1907
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-63220637-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220637
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220637
    reference: chr 2
allele count: 2
allele frequency: 1.718154015325934e-5
allele num: 116404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2842-28C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.350-28C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2734-28C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.425-28C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2947-28C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2734-28C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2842-28C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.139-28C>T
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16462
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1195
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39606
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

2-63220647-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220647
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220647
    reference: chr 2
allele count: 1
allele frequency: 8.532714427113554e-6
allele num: 117196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.350-18G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.139-18G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2734-18G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.425-18G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2734-18G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2842-18G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2842-18G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2947-18G>T
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2044
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41231
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9286
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

2-63220652-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220652
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220652
    reference: chr 2
allele count: 2
allele frequency: 1.702562356346301e-5
allele num: 117470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.139-13G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2734-13G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.425-13G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2734-13G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2947-13G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2842-13G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.350-13G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2842-13G>A
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1898
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2051
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

2-63220659-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220659
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220659
    reference: chr 2
allele count: 65
allele frequency: 5.504089962233475e-4
allele num: 118094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2734-6G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.350-6G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2947-6G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.139-6G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2842-6G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2842-6G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.425-6G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2734-6G>A
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10720
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18585
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 24568
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2054
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 3.25e1
  variant carriers: 0
hgvs: c.2947-6G>A
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

2-63220661-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220661
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220661
    reference: chr 2
allele count: 286
allele frequency: 2.417378074549911e-3
allele num: 118310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2842-4T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.139-4T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2947-4T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.425-4T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2734-4T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.350-4T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2734-4T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2842-4T>C
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 18720
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 24608
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10686
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1881
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1552
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 9.75e1
  variant carriers: 283
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
hgvs: c.2947-4T>C
num of homozygotes: 3
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

2-63220669-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220669
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220669
    reference: chr 2
allele count: 1
allele frequency: 8.412693071305987e-6
allele num: 118868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2738G>A
  hgvsp: ENSP00000403783.1:p.Gly913Asp
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.429G>A
  hgvsp: ENSP00000388442.1:p.Gly144Asp
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.354G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.143G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2846G>A
  hgvsp: ENSP00000346482.3:p.Gly949Asp
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2951G>A
  hgvsp: ENSP00000263991.5:p.Gly984Asp
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2738G>A
  hgvsp: ENSP00000384143.3:p.Gly913Asp
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2846G>A
  hgvsp: ENSP00000385524.1:p.Gly949Asp
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1272
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43226
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly984Asp
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

2-63220669-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220669
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220669
    reference: chr 2
allele count: 2
allele frequency: 1.682538614261197e-5
allele num: 118868
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2738G>T
  hgvsp: ENSP00000403783.1:p.Gly913Val
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2738G>T
  hgvsp: ENSP00000384143.3:p.Gly913Val
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.354G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2846G>T
  hgvsp: ENSP00000385524.1:p.Gly949Val
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2846G>T
  hgvsp: ENSP00000346482.3:p.Gly949Val
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2951G>T
  hgvsp: ENSP00000263991.5:p.Gly984Val
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.429G>T
  hgvsp: ENSP00000388442.1:p.Gly144Val
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.143G>T
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10769
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly984Val
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

2-63220671-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220671
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220671
    reference: chr 2
allele count: 1
allele frequency: 8.398138972403716e-6
allele num: 119074
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2740A>G
  hgvsp: ENSP00000403783.1:p.Thr914Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.431A>G
  hgvsp: ENSP00000388442.1:p.Thr145Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.145A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.356A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2848A>G
  hgvsp: ENSP00000385524.1:p.Thr950Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2848A>G
  hgvsp: ENSP00000346482.3:p.Thr950Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2740A>G
  hgvsp: ENSP00000384143.3:p.Thr914Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2953A>G
  hgvsp: ENSP00000263991.5:p.Thr985Ala
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr985Ala
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum

2-63220672-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220672
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220672
    reference: chr 2
allele count: 148
allele frequency: 1.242569768613359e-3
allele num: 119108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2741C>T
  hgvsp: ENSP00000384143.3:p.Thr914Ile
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.357C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2954C>T
  hgvsp: ENSP00000263991.5:p.Thr985Ile
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2849C>T
  hgvsp: ENSP00000385524.1:p.Thr950Ile
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.146C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2849C>T
  hgvsp: ENSP00000346482.3:p.Thr950Ile
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2741C>T
  hgvsp: ENSP00000403783.1:p.Thr914Ile
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.432C>T
  hgvsp: ENSP00000388442.1:p.Thr145Ile
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 18901
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 25207
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 10753
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43299
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr985Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

2-63220674-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220674
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220674
    reference: chr 2
allele count: 1
allele frequency: 8.384197464618687e-6
allele num: 119272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2743G>A
  hgvsp: ENSP00000403783.1:p.Glu915Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2743G>A
  hgvsp: ENSP00000384143.3:p.Glu915Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.434G>A
  hgvsp: ENSP00000388442.1:p.Glu146Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2956G>A
  hgvsp: ENSP00000263991.5:p.Glu986Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.148G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.359G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2851G>A
  hgvsp: ENSP00000385524.1:p.Glu951Lys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2851G>A
  hgvsp: ENSP00000346482.3:p.Glu951Lys
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25357
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu986Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

2-63220677-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220677
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220677
    reference: chr 2
allele count: 1
allele frequency: 8.375069094320028e-6
allele num: 119402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2854G>T
  hgvsp: ENSP00000385524.1:p.Asp952Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2854G>T
  hgvsp: ENSP00000346482.3:p.Asp952Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2959G>T
  hgvsp: ENSP00000263991.5:p.Asp987Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2746G>T
  hgvsp: ENSP00000403783.1:p.Asp916Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.437G>T
  hgvsp: ENSP00000388442.1:p.Asp147Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2746G>T
  hgvsp: ENSP00000384143.3:p.Asp916Tyr
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.362G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.151G>T
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10772
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9622
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp987Tyr
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

2-63220680-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220680
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220680
    reference: chr 2
allele count: 119
allele frequency: 9.958158995815899e-4
allele num: 119500
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.365C>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2962C>G
  hgvsp: ENSP00000263991.5:p.Leu988Val
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.154C>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.440C>G
  hgvsp: ENSP00000388442.1:p.Leu148Val
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2749C>G
  hgvsp: ENSP00000403783.1:p.Leu917Val
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2749C>G
  hgvsp: ENSP00000384143.3:p.Leu917Val
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2857C>G
  hgvsp: ENSP00000385524.1:p.Leu953Val
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2857C>G
  hgvsp: ENSP00000346482.3:p.Leu953Val
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 10784
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 25469
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19008
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43798
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu988Val
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

2-63220682-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220682
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220682
    reference: chr 2
allele count: 2
allele frequency: 1.67319211591875e-5
allele num: 119532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2751C>G
  hgvsp: ENST00000431489.1:c.2751C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2859C>G
  hgvsp: ENST00000354487.3:c.2859C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.442C>G
  hgvsp: ENST00000422032.1:c.442C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2751C>G
  hgvsp: ENST00000405015.3:c.2751C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.367C>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2964C>G
  hgvsp: ENST00000263991.5:c.2964C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2859C>G
  hgvsp: ENST00000405289.1:c.2859C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.156C>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9617
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu988Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

2-63220683-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220683
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220683
    reference: chr 2
allele count: 7
allele frequency: 5.85587846542522e-5
allele num: 119538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.368C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2860C>T
  hgvsp: ENSP00000385524.1:p.Arg954Trp
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2752C>T
  hgvsp: ENSP00000384143.3:p.Arg918Trp
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.443C>T
  hgvsp: ENSP00000388442.1:p.Arg149Trp
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.157C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2860C>T
  hgvsp: ENSP00000346482.3:p.Arg954Trp
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2752C>T
  hgvsp: ENSP00000403783.1:p.Arg918Trp
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2965C>T
  hgvsp: ENSP00000263991.5:p.Arg989Trp
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18879
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1858
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg989Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

2-63220684-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220684
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220684
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 119618
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2753G>A
  hgvsp: ENSP00000384143.3:p.Arg918Gln
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.369G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.158G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2966G>A
  hgvsp: ENSP00000263991.5:p.Arg989Gln
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.444G>A
  hgvsp: ENSP00000388442.1:p.Arg149Gln
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2861G>A
  hgvsp: ENSP00000346482.3:p.Arg954Gln
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2753G>A
  hgvsp: ENSP00000403783.1:p.Arg918Gln
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2861G>A
  hgvsp: ENSP00000385524.1:p.Arg954Gln
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 10818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2068
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43848
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9630
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg989Gln
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

2-63220684-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220684
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220684
    reference: chr 2
allele count: 1
allele frequency: 8.359945827551038e-6
allele num: 119618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.158G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2861G>T
  hgvsp: ENSP00000346482.3:p.Arg954Leu
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.444G>T
  hgvsp: ENSP00000388442.1:p.Arg149Leu
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.369G>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2753G>T
  hgvsp: ENSP00000403783.1:p.Arg918Leu
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2966G>T
  hgvsp: ENSP00000263991.5:p.Arg989Leu
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2753G>T
  hgvsp: ENSP00000384143.3:p.Arg918Leu
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2861G>T
  hgvsp: ENSP00000385524.1:p.Arg954Leu
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10818
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43848
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg989Leu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

2-63220685-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220685
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220685
    reference: chr 2
allele count: 2
allele frequency: 1.671597880413888e-5
allele num: 119646
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.159G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2862G>A
  hgvsp: ENST00000405289.1:c.2862G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2754G>A
  hgvsp: ENST00000405015.3:c.2754G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.370G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2754G>A
  hgvsp: ENST00000431489.1:c.2754G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.445G>A
  hgvsp: ENST00000422032.1:c.445G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2862G>A
  hgvsp: ENST00000354487.3:c.2862G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2967G>A
  hgvsp: ENST00000263991.5:c.2967G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2065
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1861
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg989Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

2-63220697-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220697
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220697
    reference: chr 2
allele count: 2
allele frequency: 1.667750704624673e-5
allele num: 119922
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2979A>G
  hgvsp: ENST00000263991.5:c.2979A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2874A>G
  hgvsp: ENST00000354487.3:c.2874A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2874A>G
  hgvsp: ENST00000405289.1:c.2874A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.382A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2766A>G
  hgvsp: ENST00000405015.3:c.2766A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.457A>G
  hgvsp: ENST00000422032.1:c.457A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2766A>G
  hgvsp: ENST00000431489.1:c.2766A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.171A>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43728
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu993Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

2-63220697-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220697
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220697
    reference: chr 2
allele count: 1
allele frequency: 8.338753523123364e-6
allele num: 119922
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2979A>T
  hgvsp: ENSP00000263991.5:p.Leu993Phe
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2766A>T
  hgvsp: ENSP00000403783.1:p.Leu922Phe
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2766A>T
  hgvsp: ENSP00000384143.3:p.Leu922Phe
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2874A>T
  hgvsp: ENSP00000346482.3:p.Leu958Phe
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.382A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.457A>T
  hgvsp: ENSP00000388442.1:p.Leu153Phe
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.171A>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2874A>T
  hgvsp: ENSP00000385524.1:p.Leu958Phe
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25843
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43728
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu993Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

2-63220704-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220704
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220704
    reference: chr 2
allele count: 1
allele frequency: 8.333888925928395e-6
allele num: 119992
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2773A>G
  hgvsp: ENSP00000403783.1:p.Thr925Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2773A>G
  hgvsp: ENSP00000384143.3:p.Thr925Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.464A>G
  hgvsp: ENSP00000388442.1:p.Thr156Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.389A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.178A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2986A>G
  hgvsp: ENSP00000263991.5:p.Thr996Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2881A>G
  hgvsp: ENSP00000346482.3:p.Thr961Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2881A>G
  hgvsp: ENSP00000385524.1:p.Thr961Ala
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr996Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

2-63220706-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220706
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220706
    reference: chr 2
allele count: 6
allele frequency: 5.00058340139683e-5
allele num: 119986
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2988A>G
  hgvsp: ENST00000263991.5:c.2988A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2883A>G
  hgvsp: ENST00000405289.1:c.2883A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2883A>G
  hgvsp: ENST00000354487.3:c.2883A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.180A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.391A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2775A>G
  hgvsp: ENST00000405015.3:c.2775A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2775A>G
  hgvsp: ENST00000431489.1:c.2775A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.466A>G
  hgvsp: ENST00000422032.1:c.466A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr996Thr
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

2-63220707-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220707
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220707
    reference: chr 2
allele count: 1
allele frequency: 8.334583520861462e-6
allele num: 119982
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.467A>G
  hgvsp: ENSP00000388442.1:p.Thr157Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2776A>G
  hgvsp: ENSP00000403783.1:p.Thr926Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2884A>G
  hgvsp: ENSP00000346482.3:p.Thr962Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.392A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.181A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2989A>G
  hgvsp: ENSP00000263991.5:p.Thr997Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2884A>G
  hgvsp: ENSP00000385524.1:p.Thr962Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2776A>G
  hgvsp: ENSP00000384143.3:p.Thr926Ala
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr997Ala
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP

2-63220713-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220713
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220713
    reference: chr 2
allele count: 2
allele frequency: 1.667639456349537e-5
allele num: 119930
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2890C>G
  hgvsp: ENSP00000346482.3:p.Arg964Gly
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2782C>G
  hgvsp: ENSP00000403783.1:p.Arg928Gly
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.473C>G
  hgvsp: ENSP00000388442.1:p.Arg159Gly
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2782C>G
  hgvsp: ENSP00000384143.3:p.Arg928Gly
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.187C>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2995C>G
  hgvsp: ENSP00000263991.5:p.Arg999Gly
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.398C>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2890C>G
  hgvsp: ENSP00000385524.1:p.Arg964Gly
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43694
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1811
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Arg999Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

2-63220713-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220713
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220713
    reference: chr 2
allele count: 40
allele frequency: 3.335278912699075e-4
allele num: 119930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.473C>T
  hgvsp: ENSP00000388442.1:p.Arg159Cys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2782C>T
  hgvsp: ENSP00000403783.1:p.Arg928Cys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2995C>T
  hgvsp: ENSP00000263991.5:p.Arg999Cys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2782C>T
  hgvsp: ENSP00000384143.3:p.Arg928Cys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2890C>T
  hgvsp: ENSP00000385524.1:p.Arg964Cys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2890C>T
  hgvsp: ENSP00000346482.3:p.Arg964Cys
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.398C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.187C>T
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18557
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10807
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 9511
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1811
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 9.75e1
  variant carriers: 40
hgvs: p.Arg999Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-63220714-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220714
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220714
    reference: chr 2
allele count: 8
allele frequency: 6.671559143371805e-5
allele num: 119912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2783G>A
  hgvsp: ENSP00000384143.3:p.Arg928His
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2891G>A
  hgvsp: ENSP00000385524.1:p.Arg964His
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2783G>A
  hgvsp: ENSP00000403783.1:p.Arg928His
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2891G>A
  hgvsp: ENSP00000346482.3:p.Arg964His
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.474G>A
  hgvsp: ENSP00000388442.1:p.Arg159His
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.399G>A
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2996G>A
  hgvsp: ENSP00000263991.5:p.Arg999His
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.188G>A
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9522
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg999His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

2-63220717-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220717
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220717
    reference: chr 2
allele count: 1
allele frequency: 8.34153584357952e-6
allele num: 119882
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2894T>C
  hgvsp: ENSP00000385524.1:p.Phe965Ser
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.2999T>C
  hgvsp: ENSP00000263991.5:p.Phe1000Ser
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2786T>C
  hgvsp: ENSP00000384143.3:p.Phe929Ser
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.477T>C
  hgvsp: ENSP00000388442.1:p.Phe160Ser
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2786T>C
  hgvsp: ENSP00000403783.1:p.Phe929Ser
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2894T>C
  hgvsp: ENSP00000346482.3:p.Phe965Ser
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.191T>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.402T>C
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 25833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43561
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9521
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Phe1000Ser
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/2-63220742-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220742
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220742
    reference: chr 2
allele count: 1
allele frequency: 8.361903169161301e-6
allele num: 119590
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2919A>C
  hgvsp: ENSP00000346482.3:p.Lys973Asn
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2811A>C
  hgvsp: ENSP00000384143.3:p.Lys937Asn
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2919A>C
  hgvsp: ENSP00000385524.1:p.Lys973Asn
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.3024A>C
  hgvsp: ENSP00000263991.5:p.Lys1008Asn
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2811A>C
  hgvsp: ENSP00000403783.1:p.Lys937Asn
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.427A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.502A>C
  hgvsp: ENSP00000388442.1:p.Lys168Asn
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.216A>C
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44006
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys1008Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

2-63220749-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220749
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220749
    reference: chr 2
allele count: 1
allele frequency: 8.370442294170824e-6
allele num: 119468
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.434A>G
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.3031A>G
  hgvsp: ENSP00000263991.5:p.Thr1011Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2926A>G
  hgvsp: ENSP00000346482.3:p.Thr976Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2926A>G
  hgvsp: ENSP00000385524.1:p.Thr976Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.509A>G
  hgvsp: ENSP00000388442.1:p.Thr171Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2818A>G
  hgvsp: ENSP00000403783.1:p.Thr940Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2818A>G
  hgvsp: ENSP00000384143.3:p.Thr940Ala
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.223A>G
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9404
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr1011Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

2-63220774-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220774
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220774
    reference: chr 2
allele count: 4
allele frequency: 3.368137420006736e-5
allele num: 118760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2843C>T
  hgvsp: ENSP00000403783.1:p.Ser948Phe
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.3056C>T
  hgvsp: ENSP00000263991.5:p.Ser1019Phe
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2843C>T
  hgvsp: ENSP00000384143.3:p.Ser948Phe
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.459C>T
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2951C>T
  hgvsp: ENSP00000385524.1:p.Ser984Phe
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.534C>T
  hgvsp: ENSP00000388442.1:p.Ser179Phe
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2951C>T
  hgvsp: ENSP00000346482.3:p.Ser984Phe
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.248C>T
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25709
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43942
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser1019Phe
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/2-63220783-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63220783
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63220783
    reference: chr 2
allele count: 10
allele frequency: 8.452799567216662e-5
allele num: 118304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000388442
  ensembl transcript: ENST00000422032
  gene symbol: EHBP1
  hgvsc: ENST00000422032.1:c.543A>C
  hgvsp: ENSP00000388442.1:p.Gln182Pro
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000263991
  ensembl transcript: ENST00000263991
  gene symbol: EHBP1
  hgvsc: ENST00000263991.5:c.3065A>C
  hgvsp: ENSP00000263991.5:p.Gln1022Pro
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000496857
  gene symbol: EHBP1
  hgvsc: ENST00000496857.1:n.468A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000403783
  ensembl transcript: ENST00000431489
  gene symbol: EHBP1
  hgvsc: ENST00000431489.1:c.2852A>C
  hgvsp: ENSP00000403783.1:p.Gln951Pro
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000346482
  ensembl transcript: ENST00000354487
  gene symbol: EHBP1
  hgvsc: ENST00000354487.3:c.2960A>C
  hgvsp: ENSP00000346482.3:p.Gln987Pro
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115504
  ensembl transcript: ENST00000491965
  gene symbol: EHBP1
  hgvsc: ENST00000491965.1:n.257A>C
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000385524
  ensembl transcript: ENST00000405289
  gene symbol: EHBP1
  hgvsc: ENST00000405289.1:c.2960A>C
  hgvsp: ENSP00000385524.1:p.Gln987Pro
  variant of: http://identifiers.org/hgnc/29144
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115504
  ensembl protein: ENSP00000384143
  ensembl transcript: ENST00000405015
  gene symbol: EHBP1
  hgvsc: ENST00000405015.3:c.2852A>C
  hgvsp: ENSP00000384143.3:p.Gln951Pro
  variant of: http://identifiers.org/hgnc/29144
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln1022Pro
num of homozygotes: 0
reference allele: A

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

GenotypeQuality
all individuals: 2739
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40912
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1852
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2096
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6851
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
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: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.035e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.974e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e-1

FS
type: SiteQuality
SIO_000300: 6.18e-1

DP
type: SiteQuality
SIO_000300: 1.587991e6

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

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

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1852
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6851
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40903
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2095
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.732201628269531e-4
allele num: 11546
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

DP
type: SiteQuality
SIO_000300: 1.588014e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

FS
type: SiteQuality
SIO_000300: 8.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.707e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 7.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.361e1

GenotypeQuality
all individuals: 4267
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2093
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40726
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2730
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1850
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
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: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.605e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

DP
type: SiteQuality
SIO_000300: 1.586027e6

QD
type: SiteQuality
SIO_000300: 1.538e1

GenotypeQuality
all individuals: 264
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2088
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2727
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6822
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
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: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.677542519958348e-5
allele num: 11524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.496e0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.585335e6

MQRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.85e-1

QD
type: SiteQuality
SIO_000300: 1.572e1

MQ
type: SiteQuality
SIO_000300: 5.979e1

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

GenotypeQuality
all individuals: 1851
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6821
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2727
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4266
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2087
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1012
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.683570684265369e-5
allele num: 11516
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.906e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 3.218e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.17e-1

MQ
type: SiteQuality
SIO_000300: 5.893e1

DP
type: SiteQuality
SIO_000300: 1.584262e6

MQRankSum
type: SiteQuality
SIO_000300: -7.55e-1

QD
type: SiteQuality
SIO_000300: 1.325e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

GenotypeQuality
all individuals: 6809
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40475
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1850
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66562
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.583253e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.389e0

VQSLOD
type: SiteQuality
SIO_000300: 9.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

QD
type: SiteQuality
SIO_000300: 1.37e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

FS
type: SiteQuality
SIO_000300: 3.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.967e1

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

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39762
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4268
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6770
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1012
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66436
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.766e-1

QD
type: SiteQuality
SIO_000300: 7.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.09e-1

DP
type: SiteQuality
SIO_000300: 1.578784e6

MQ
type: SiteQuality
SIO_000300: 5.943e1

FS
type: SiteQuality
SIO_000300: 4.892e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.75e-1

GenotypeQuality
all individuals: 183
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1012
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1843
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39628
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-1

QD
type: SiteQuality
SIO_000300: 1.219e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.619e0

FS
type: SiteQuality
SIO_000300: 3.845e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.549e0

DP
type: SiteQuality
SIO_000300: 1.577391e6

VQSLOD
type: SiteQuality
SIO_000300: 8.92e-1

GenotypeQuality
all individuals: 6740
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 35

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 84
bin: 5.75e1
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GenotypeQuality
all individuals: 39242
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.744287458573173e-4
allele num: 11466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

African
type: Population
allele count: 32
allele frequency: 3.094179075614001e-3
allele num: 10342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66370
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

QD
type: SiteQuality
SIO_000300: 1.362e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.264e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

DP
type: SiteQuality
SIO_000300: 1.576744e6

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
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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: 900
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.721437292865864e-5
allele num: 11466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.264e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.576744e6

QD
type: SiteQuality
SIO_000300: 1.362e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66216
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.639999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.736e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

DP
type: SiteQuality
SIO_000300: 1.562696e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.631e0

MQRankSum
type: SiteQuality
SIO_000300: 2.98e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.215657670799903e-4
allele num: 16452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66064
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8366
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

QD
type: SiteQuality
SIO_000300: 1.531e1

VQSLOD
type: SiteQuality
SIO_000300: 4.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.537063e6

GenotypeQuality
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bin: 9.25e1
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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.796238244514106e-5
allele num: 10208
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.035e1

FS
type: SiteQuality
SIO_000300: 4.105e0

MQRankSum
type: SiteQuality
SIO_000300: 9.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

DP
type: SiteQuality
SIO_000300: 2.249406e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.536e0

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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variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.514233797698365e-4
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66480
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: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 5.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.27e-1

QD
type: SiteQuality
SIO_000300: 1.496e1

DP
type: SiteQuality
SIO_000300: 2.253244e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

FS
type: SiteQuality
SIO_000300: 1.175e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.489e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.085e1

FS
type: SiteQuality
SIO_000300: 1.0173e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -9.108000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.986e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 2.262452e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e-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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503804625703029e-5
allele num: 66498
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.0173e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -9.54e-1

QD
type: SiteQuality
SIO_000300: 1.085e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -9.108000000000001e-1

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.986e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 2.262452e6

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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African
type: Population
allele count: 1
allele frequency: 9.721952167995334e-5
allele num: 10286
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
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QD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4872
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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: 1
allele frequency: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

QD
type: SiteQuality
SIO_000300: 1.893e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

FS
type: SiteQuality
SIO_000300: 2.153e0

DP
type: SiteQuality
SIO_000300: 2.270159e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4861
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18739
bin: 9.75e1
variant carriers: 8

African
type: Population
allele count: 7
allele frequency: 6.782945736434108e-4
allele num: 10320
num of homozygotes: 0

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 1.308e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

DP
type: SiteQuality
SIO_000300: 2.273356e6

FS
type: SiteQuality
SIO_000300: 2.702e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.86e-1

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4654
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2324
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

DP
type: SiteQuality
SIO_000300: 2.276927e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

QD
type: SiteQuality
SIO_000300: 1.378e1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

GenotypeQuality
all individuals: 161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15806
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4866
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variant carriers: 0

GenotypeQuality
all individuals: 4654
bin: 8.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.088e0

VQSLOD
type: SiteQuality
SIO_000300: -4.506e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 3.919e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.312e1

DP
type: SiteQuality
SIO_000300: 2.278244e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.519e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.301e0

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18728
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4866
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 2324
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

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

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 6927
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.57e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.771e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 2.278317e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.22e-1

QD
type: SiteQuality
SIO_000300: 1.381e1

FS
type: SiteQuality
SIO_000300: 6.266e0

GenotypeQuality
all individuals: 6932
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15910
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4649
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4861
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.97e-1

DP
type: SiteQuality
SIO_000300: 2.279089e6

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.615e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.14e-1

QD
type: SiteQuality
SIO_000300: 9.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27
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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: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2322
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.279775e6

VQSLOD
type: SiteQuality
SIO_000300: 8.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

FS
type: SiteQuality
SIO_000300: 3.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.2e0

MQRankSum
type: SiteQuality
SIO_000300: 8.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.286e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
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GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15947
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 4647
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.171783454417624e-4
allele num: 8534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.877e-1

FS
type: SiteQuality
SIO_000300: 7.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.107e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.77e-1

DP
type: SiteQuality
SIO_000300: 2.279716e6

QD
type: SiteQuality
SIO_000300: 1.326e1

GenotypeQuality
all individuals: 2322
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
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variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 3140
bin: 7.25e1
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GenotypeQuality
all individuals: 15854
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21256214380987e-4
allele num: 16494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.36e0

DP
type: SiteQuality
SIO_000300: 2.278429e6

QD
type: SiteQuality
SIO_000300: 1.491e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.296e0

FS
type: SiteQuality
SIO_000300: 2.057e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18722
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3139
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 41
bin: 7.5e0
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GenotypeQuality
all individuals: 2322
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GenotypeQuality
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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: 4638
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.692628650904033e-5
allele num: 11504
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8532
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

VQSLOD
type: SiteQuality
SIO_000300: 2.78e-1

BaseQRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.277814e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
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SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.626e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

European (Finnish)
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allele count: 10
allele frequency: 1.514233797698365e-3
allele num: 6604
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.05e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.705e1

VQSLOD
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MQRankSum
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SIO_000300: -1.004e0

FS
type: SiteQuality
SIO_000300: 6.33e-1

DP
type: SiteQuality
SIO_000300: 2.272834e6

QD
type: SiteQuality
SIO_000300: 1.343e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
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: 0
allele frequency: 0.0e0
allele num: 66546
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

DP
type: SiteQuality
SIO_000300: 2.269936e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 6.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.25e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

QD
type: SiteQuality
SIO_000300: 1.342e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.48e-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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.404351876897184e-4
allele num: 66546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 1.342e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

FS
type: SiteQuality
SIO_000300: 6.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.39e-1

DP
type: SiteQuality
SIO_000300: 2.269936e6

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.011060351045924e-5
allele num: 66544
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.77e-1

FS
type: SiteQuality
SIO_000300: 5.563e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.18e-2

QD
type: SiteQuality
SIO_000300: 1.222e1

DP
type: SiteQuality
SIO_000300: 2.268699e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.759e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.149999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeQuality
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bin: 7.25e1
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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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.701457451810061e-4
allele num: 8508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66476
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 2.247701e6

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.86e-1

BaseQRankSum
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SIO_000300: -3.642e0

FS
type: SiteQuality
SIO_000300: 8.84e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 9.789999999999999e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
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East Asian
type: Population
allele count: 0
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allele num: 8504
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South Asian
type: Population
allele count: 1
allele frequency: 6.151574803149606e-5
allele num: 16256
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66468
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.36e-1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.604e1

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: 735
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.741250217656277e-4
allele num: 11486
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66476
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8504
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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: 904
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South Asian
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.403e1

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 5.89e-1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.34e0

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

DP
type: SiteQuality
SIO_000300: 2.241117e6

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504528631179851e-5
allele num: 66466
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8498
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16256
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
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Other
type: Population
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

QD
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MQ
type: SiteQuality
SIO_000300: 5.805e1

MQRankSum
type: SiteQuality
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FS
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.252e0

DP
type: SiteQuality
SIO_000300: 2.232747e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 244
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66474
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.13195977434388e-5
allele num: 16308
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.360000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

QD
type: SiteQuality
SIO_000300: 1.324e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

DP
type: SiteQuality
SIO_000300: 2.232307e6

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 5.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505117399157134e-5
allele num: 66440
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.975e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-2

QD
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SIO_000300: 1.114e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.47e-1

DP
type: SiteQuality
SIO_000300: 2.21721e6

GenotypeQuality
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bin: 1.25e1
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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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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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.94325689856199e-4
allele num: 10292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16164
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: 66372
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.738203425375742e-5
allele num: 11444
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

QD
type: SiteQuality
SIO_000300: 1.318e1

MQRankSum
type: SiteQuality
SIO_000300: 3.51e-1

DP
type: SiteQuality
SIO_000300: 2.198271e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e0

FS
type: SiteQuality
SIO_000300: 1.403e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

GenotypeQuality
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bin: 7.25e1
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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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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variant carriers: 1

GenotypeQuality
all individuals: 659
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65208
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.004217714400482e-4
allele num: 9958
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11336
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.849e1

DP
type: SiteQuality
SIO_000300: 1.531244e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

QD
type: SiteQuality
SIO_000300: 1.122e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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
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GenotypeQuality
all individuals: 487
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.067955207853965e-5
allele num: 65190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13502
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.032e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

DP
type: SiteQuality
SIO_000300: 1.540716e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.05e-1

GenotypeQuality
all individuals: 868
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13560
num of homozygotes: 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: 9968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.181474480151229e-4
allele num: 8464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65244
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.015e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.736e0

VQSLOD
type: SiteQuality
SIO_000300: -1.297e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

DP
type: SiteQuality
SIO_000300: 1.549153e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.19e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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
all individuals: 294
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variant carriers: 0

GenotypeQuality
all individuals: 2337
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.060350104051904e-5
allele num: 65352
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.52e-1

FS
type: SiteQuality
SIO_000300: 9.16e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.954e0

QD
type: SiteQuality
SIO_000300: 8.220000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -5.276999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.566025e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

GenotypeQuality
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bin: 7.5e0
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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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 792
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525739220652406e-5
allele num: 65542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.261e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.193e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 2.173e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.03e-1

DP
type: SiteQuality
SIO_000300: 1.584179e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 148
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GenotypeQuality
all individuals: 41579
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.178411501296253e-4
allele num: 8486
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.796622097114708e-5
allele num: 11368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65626
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.130000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

DP
type: SiteQuality
SIO_000300: 1.590529e6

VQSLOD
type: SiteQuality
SIO_000300: 2.9e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 320
bin: 2.75e1
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GenotypeQuality
all individuals: 577
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variant carriers: 62

GenotypeQuality
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GenotypeQuality
all individuals: 24
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 602
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variant carriers: 1

GenotypeQuality
all individuals: 110
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GenotypeQuality
all individuals: 164
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GenotypeQuality
all individuals: 1905
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variant carriers: 0

GenotypeQuality
all individuals: 1643
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.1441647597254e-3
allele num: 874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.153305203938116e-4
allele num: 11376
num of homozygotes: 0

African
type: Population
allele count: 53
allele frequency: 5.224763406940063e-3
allele num: 10144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.013422818791946e-4
allele num: 14900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520496289989052e-5
allele num: 65768
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

FS
type: SiteQuality
SIO_000300: 1.784e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

DP
type: SiteQuality
SIO_000300: 1.602594e6

QD
type: SiteQuality
SIO_000300: 1.211e1

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

GenotypeQuality
all individuals: 422
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2049
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 7.5e0
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GenotypeQuality
all individuals: 290
bin: 2.75e1
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GenotypeQuality
all individuals: 9421
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
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GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42690
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variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 247
allele frequency: 3.752544741879615e-3
allele num: 65822
num of homozygotes: 3

African
type: Population
allele count: 4
allele frequency: 3.938558487593541e-4
allele num: 10156
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.545454545454545e-3
allele num: 880
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.222867624579639e-3
allele num: 6542
num of homozygotes: 0

Latino
type: Population
allele count: 21
allele frequency: 1.845342706502636e-3
allele num: 11380
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.329787234042553e-4
allele num: 15040
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.55e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.610109e6

QD
type: SiteQuality
SIO_000300: 1.397e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

GenotypeQuality
all individuals: 197
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 20
bin: 2.5e0
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GenotypeQuality
all individuals: 9523
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
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GenotypeQuality
all individuals: 1890
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variant carriers: 0

GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 400
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variant carriers: 1

GenotypeQuality
all individuals: 571
bin: 8.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.177578897786152e-4
allele num: 8492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65950
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15426
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.436e0

VQSLOD
type: SiteQuality
SIO_000300: 6.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.233e0

DP
type: SiteQuality
SIO_000300: 1.609267e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

FS
type: SiteQuality
SIO_000300: 4.138e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.059e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 9523
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 109
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 113
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GenotypeQuality
all individuals: 571
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
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GenotypeQuality
all individuals: 43226
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variant carriers: 0

GenotypeQuality
all individuals: 2061
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 2.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.032600454890068e-5
allele num: 65950
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15426
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.138e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.059e1

DP
type: SiteQuality
SIO_000300: 1.609267e6

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.233e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.436e0

VQSLOD
type: SiteQuality
SIO_000300: 6.38e-1

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
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variant carriers: 0

GenotypeQuality
all individuals: 9564
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variant carriers: 0

GenotypeQuality
all individuals: 117
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variant carriers: 0

GenotypeQuality
all individuals: 573
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variant carriers: 0

GenotypeQuality
all individuals: 2075
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variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
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GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
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variant carriers: 0

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

GenotypeQuality
all individuals: 43475
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.807767752059631e-5
allele num: 10196
num of homozygotes: 0

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

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: 15572
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65992
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.96e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.699e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: -2.366e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

QD
type: SiteQuality
SIO_000300: 1.584e1

FS
type: SiteQuality
SIO_000300: 1.097e0

DP
type: SiteQuality
SIO_000300: 1.611411e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.25e0

GenotypeQuality
all individuals: 9544
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
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variant carriers: 0

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

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 496
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variant carriers: 147

GenotypeQuality
all individuals: 191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
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variant carriers: 0

GenotypeQuality
all individuals: 185
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GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2060
bin: 7.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 129
allele frequency: 1.954663919025395e-3
allele num: 65996
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 12
allele frequency: 1.831501831501832e-3
allele num: 6552
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 5.884660651235779e-4
allele num: 10196
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15604
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.787346221441125e-5
allele num: 11380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.82e-1

DP
type: SiteQuality
SIO_000300: 1.6155e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.77e0

QD
type: SiteQuality
SIO_000300: 1.126e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.372e0

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

GenotypeQuality
all individuals: 281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9607
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variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
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variant carriers: 0

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

GenotypeQuality
all individuals: 205
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
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variant carriers: 0

GenotypeQuality
all individuals: 43577
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1879
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2074
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.356470887363335e-5
allele num: 15732
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66020
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.464e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 7.81e0

FS
type: SiteQuality
SIO_000300: 4.03e0

MQRankSum
type: SiteQuality
SIO_000300: 7.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.213e-1

DP
type: SiteQuality
SIO_000300: 1.613169e6

GenotypeQuality
all individuals: 2081
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 7.5e0
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GenotypeQuality
all individuals: 156
bin: 3.75e1
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GenotypeQuality
all individuals: 1021
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
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GenotypeQuality
all individuals: 117
bin: 5.25e1
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GenotypeQuality
all individuals: 137
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variant carriers: 0

GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 43799
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GenotypeQuality
all individuals: 351
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variant carriers: 1

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1879
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66054
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.321911746112024e-5
allele num: 15818
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.085e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.792e0

FS
type: SiteQuality
SIO_000300: 2.321e0

MQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.19e-1

DP
type: SiteQuality
SIO_000300: 1.614901e6

GenotypeQuality
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 9.75e1
variant carriers: 119

GenotypeQuality
all individuals: 2065
bin: 7.25e1
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GenotypeQuality
all individuals: 543
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GenotypeQuality
all individuals: 129
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GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 972
bin: 2.25e1
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GenotypeQuality
all individuals: 129
bin: 4.75e1
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GenotypeQuality
all individuals: 72
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GenotypeQuality
all individuals: 9602
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.515556336790297e-4
allele num: 11378
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.194217473287241e-3
allele num: 15910
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: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.121076233183856e-3
allele num: 892
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.935995302407516e-4
allele num: 10218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 92
allele frequency: 1.392631164663498e-3
allele num: 66062
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.26e0

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.68e-1

FS
type: SiteQuality
SIO_000300: 1.102e0

QD
type: SiteQuality
SIO_000300: 1.348e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-2

DP
type: SiteQuality
SIO_000300: 1.618843e6

GenotypeQuality
all individuals: 319
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variant carriers: 2

GenotypeQuality
all individuals: 2072
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GenotypeQuality
all individuals: 172
bin: 2.75e1
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GenotypeQuality
all individuals: 130
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GenotypeQuality
all individuals: 158
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GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 963
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GenotypeQuality
all individuals: 143
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43712
bin: 6.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.0274590536163e-5
allele num: 66062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.51e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.31e-1

QD
type: SiteQuality
SIO_000300: 1.803e1

FS
type: SiteQuality
SIO_000300: 2.524e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.22e-1

DP
type: SiteQuality
SIO_000300: 1.616601e6

MQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 9.75e1
variant carriers: 7

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513912859175826e-5
allele num: 66054
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.110601894286587e-4
allele num: 6546
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.792401096748923e-5
allele num: 10212
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.259389083625437e-5
allele num: 15976
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.046e1

FS
type: SiteQuality
SIO_000300: 1.137e0

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.01e-1

DP
type: SiteQuality
SIO_000300: 1.617865e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-1

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66090
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.618328e6

QD
type: SiteQuality
SIO_000300: 5.17e0

VQSLOD
type: SiteQuality
SIO_000300: -1.925e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

FS
type: SiteQuality
SIO_000300: 1.316e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

GenotypeQuality
all individuals: 316
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
all individuals: 1859
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GenotypeQuality
all individuals: 2068
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51308821304282e-5
allele num: 66090
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16016
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.316e0

MQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

DP
type: SiteQuality
SIO_000300: 1.618328e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 5.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.925e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

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

GenotypeQuality
all individuals: 315
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variant carriers: 2

GenotypeQuality
all individuals: 163
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16040
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.025901718712176e-5
allele num: 66096
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-2

QD
type: SiteQuality
SIO_000300: 1.587e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

FS
type: SiteQuality
SIO_000300: 3.232e0

DP
type: SiteQuality
SIO_000300: 1.618455e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.381e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.37e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.23e-1

GenotypeQuality
all individuals: 1838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.784735812133073e-5
allele num: 10220
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.13195977434388e-5
allele num: 16308
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: 8474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.11e-1

FS
type: SiteQuality
SIO_000300: 5.89e-1

QD
type: SiteQuality
SIO_000300: 1.493e1

DP
type: SiteQuality
SIO_000300: 1.621309e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.23e-1

GenotypeQuality
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bin: 4.75e1
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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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.180080245456691e-4
allele num: 8474
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: 5.946e1

MQRankSum
type: SiteQuality
SIO_000300: -3.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

FS
type: SiteQuality
SIO_000300: 5.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

QD
type: SiteQuality
SIO_000300: 1.493e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

DP
type: SiteQuality
SIO_000300: 1.621309e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.11e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 208
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66116
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.110228522546743e-5
allele num: 16366
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 9.9e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

DP
type: SiteQuality
SIO_000300: 1.621687e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

FS
type: SiteQuality
SIO_000300: 9.94e0

VQSLOD
type: SiteQuality
SIO_000300: -8.111e-1

GenotypeQuality
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bin: 6.25e1
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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variant carriers: 6

GenotypeQuality
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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: 2030
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GenotypeQuality
all individuals: 198
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.720320981826764e-4
allele num: 8474
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66106
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.761804087385483e-4
allele num: 11352
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.621445e6

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

QD
type: SiteQuality
SIO_000300: 1.385e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e-1

FS
type: SiteQuality
SIO_000300: 5.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.42e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 146
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GenotypeQuality
all individuals: 2031
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43950
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512950859356088e-5
allele num: 66096
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.75e0

VQSLOD
type: SiteQuality
SIO_000300: -9.188e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.09e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.825e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

DP
type: SiteQuality
SIO_000300: 1.620966e6

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.027184113337773e-5
allele num: 66068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

QD
type: SiteQuality
SIO_000300: 1.28e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.51e-1

DP
type: SiteQuality
SIO_000300: 1.621079e6

FS
type: SiteQuality
SIO_000300: 5.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 4.47e0

GenotypeQuality
all individuals: 43694
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2012
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.25e1
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GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 524
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GenotypeQuality
all individuals: 103
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.221597849987784e-4
allele num: 16372
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.805917576611483e-5
allele num: 11356
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.054368226675546e-5
allele num: 66068
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

African
type: Population
allele count: 33
allele frequency: 3.227699530516432e-3
allele num: 10224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 5.23e-1

QD
type: SiteQuality
SIO_000300: 1.28e1

VQSLOD
type: SiteQuality
SIO_000300: 4.47e0

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

DP
type: SiteQuality
SIO_000300: 1.621079e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

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

GenotypeQuality
all individuals: 210
bin: 3.25e1
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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
all individuals: 285
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
all individuals: 2006
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 843
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1803
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514050387596899e-5
allele num: 66048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.847974955977304e-4
allele num: 10222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.619423e6

QD
type: SiteQuality
SIO_000300: 1.338e1

FS
type: SiteQuality
SIO_000300: 1.727e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

GenotypeQuality
all individuals: 118
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
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variant carriers: 0

GenotypeQuality
all individuals: 119
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GenotypeQuality
all individuals: 120
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GenotypeQuality
all individuals: 2016
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GenotypeQuality
all individuals: 330
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 1804
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 221
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GenotypeQuality
all individuals: 521
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GenotypeQuality
all individuals: 200
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51437138443832e-5
allele num: 66034
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.871e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

DP
type: SiteQuality
SIO_000300: 1.61775e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.522e0

QD
type: SiteQuality
SIO_000300: 3.21e0

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9450
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 271
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variant carriers: 1

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 507
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variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65872
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.182592242194891e-4
allele num: 8456
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11308
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.781e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.481e0

QD
type: SiteQuality
SIO_000300: 3.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

DP
type: SiteQuality
SIO_000300: 1.615866e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

GenotypeQuality
all individuals: 1760
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 113
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GenotypeQuality
all individuals: 1961
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519572088499878e-5
allele num: 65808
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.29e-1

FS
type: SiteQuality
SIO_000300: 1.163e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

QD
type: SiteQuality
SIO_000300: 1.33e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.79e-1

DP
type: SiteQuality
SIO_000300: 1.614628e6

MQ
type: SiteQuality
SIO_000300: 5.945e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

GenotypeQuality
all individuals: 145
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9296
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 5.25e1
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GenotypeQuality
all individuals: 98
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GenotypeQuality
all individuals: 480
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GenotypeQuality
all individuals: 272
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1882
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variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.553028957186001e-4
allele num: 11258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.53e-1

FS
type: SiteQuality
SIO_000300: 3.548e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.648e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.09e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

QD
type: SiteQuality
SIO_000300: 1.025e1

VQSLOD
type: SiteQuality
SIO_000300: 3.47e-1

DP
type: SiteQuality
SIO_000300: 1.606188e6