2-127809972-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127809972
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127809972
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 17652
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-1484C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-1153C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-34C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.4096C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-1153C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-1484C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1135-34C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1264-34C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-34C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-1153C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-1153C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-34C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-1153C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-1153C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19242
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29061
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD

2-127809975-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127809975
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127809975
    reference: chr 2
allele count: 3
allele frequency: 1.912045889101338e-4
allele num: 15690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-1156G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-1487G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-1156G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1264-37G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-37G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-1156G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-1487G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-37G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-1156G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-37G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-1156G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1135-37G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-1156G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.4093G>C
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29375
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19141
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

2-127809975-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127809975
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127809975
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 15690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-1156G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-1487G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-1156G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1264-37G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-1156G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-1156G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-1487G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.4093G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-37G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-1156G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-1156G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1135-37G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-37G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-37G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29375
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19141
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP

2-127809985-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127809985
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127809985
    reference: chr 2
allele count: 1
allele frequency: 6.786102062975027e-5
allele num: 14736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-1497C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.4083C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-1166C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-47C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-1166C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-1497C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1135-47C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-47C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-47C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-1166C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1264-47C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-1166C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-1166C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-1166C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29978
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

2-127809985-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127809985
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127809985
    reference: chr 2
allele count: 1
allele frequency: 6.786102062975027e-5
allele num: 14736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-47C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-47C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1264-47C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-1166C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-1497C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-1166C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.4083C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-1166C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-1166C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-1166C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-1166C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1135-47C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-47C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-1497C>G
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19239
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29978
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

2-127809988-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127809988
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127809988
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 14788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-1500C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-1169C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-50C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-50C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-1169C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1264-50C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1135-50C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-1500C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-1169C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-1169C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.4080C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-1169C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-50C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-1169C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 19278
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30058
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

2-127810947-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127810947
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127810947
    reference: chr 2
allele count: 2
allele frequency: 1.718656010999398e-5
allele num: 116370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3121G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2128G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2128G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1009G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2459G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2128G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1263+51G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2128G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2459G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1134+51G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1009G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2128G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1009G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2128G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6040
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13460
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9571
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

2-127810948-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127810948
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127810948
    reference: chr 2
allele count: 3
allele frequency: 2.578116943384552e-5
allele num: 116364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1010C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2129C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2129C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2460C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3120C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1134+50C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2129C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1010C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2460C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1263+50C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2129C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2129C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1010C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2129C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9289
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13715
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP

2-127810949-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127810949
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127810949
    reference: chr 2
allele count: 3
allele frequency: 2.572634034233184e-5
allele num: 116612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2130C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2130C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2130C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3119C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2130C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2130C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1011C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1263+49C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2461C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2130C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1011C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1011C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1134+49C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2461C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12789
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/2-127810951-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127810951
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127810951
    reference: chr 2
allele count: 3
allele frequency: 2.570077445000343e-5
allele num: 116728
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1013T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1134+47T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2132T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3117T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2463T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1013T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2132T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1263+47T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1013T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2132T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2132T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2463T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2132T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2132T>G
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14519
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

2-127810959-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127810959
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127810959
    reference: chr 2
allele count: 1
allele frequency: 8.584427847883938e-6
allele num: 116490
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2140A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3109A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1263+39A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2471A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2140A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1021A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2471A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2140A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2140A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1021A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2140A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1021A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2140A>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1134+39A>G
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

2-127810960-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127810960
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127810960
    reference: chr 2
allele count: 4
allele frequency: 3.435953820780649e-5
allele num: 116416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1022G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2141G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2141G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2141G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3108G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1134+38G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1263+38G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1022G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2141G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2472G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2141G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2472G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1022G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2141G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5957
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-127810965-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127810965
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127810965
    reference: chr 2
allele count: 4
allele frequency: 3.463623296330291e-5
allele num: 115486
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2477T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1027T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2477T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1027T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3103T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1263+33T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2146T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2146T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2146T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1027T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2146T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2146T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1134+33T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2146T>G
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13387
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

2-127810967-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127810967
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127810967
    reference: chr 2
allele count: 5
allele frequency: 4.285959197668438e-5
allele num: 116660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1029C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2148C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2148C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3101C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2148C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1029C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2148C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2479C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2148C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1263+31C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2148C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2479C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1029C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1134+31C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13579
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

2-127810981-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127810981
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127810981
    reference: chr 2
allele count: 2
allele frequency: 1.712680687812564e-5
allele num: 116776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2162C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1043C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1263+17C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1134+17C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2162C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2162C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2493C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1043C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3087C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2162C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1043C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2162C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2493C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2162C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

2-127810986-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127810986
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127810986
    reference: chr 2
allele count: 7
allele frequency: 5.99294544707373e-5
allele num: 116804
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1263+12G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2167G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2167G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2167G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1048G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3082G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1134+12G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2167G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1048G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1048G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2167G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2167G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2498G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2498G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20988
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-127810987-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127810987
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127810987
    reference: chr 2
allele count: 1096
allele frequency: 9.380830922505435e-3
allele num: 116834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3081C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2499C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2168C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2168C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2168C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2168C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2499C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1263+11C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2168C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1049C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1049C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2168C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1049C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1134+11C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 1.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 20822
  bin: 2.25e1
  variant carriers: 152
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 14357
  bin: 2.75e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 1.75e1
  variant carriers: 119
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 3.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 3.25e1
  variant carriers: 138
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 9
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

2-127810991-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127810991
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127810991
    reference: chr 2
allele count: 1
allele frequency: 8.556515786771626e-6
allele num: 116870
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1053T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3077T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2172T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2172T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1053T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2172T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2172T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2503T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2172T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1134+7T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2503T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1263+7T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1053T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2172T>C
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14716
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.1263+7T>C
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

2-127811015-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811015
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811015
    reference: chr 2
allele count: 1
allele frequency: 8.5966782435267e-6
allele num: 116324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2196C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1117C>T
  hgvsp: ENSP00000350654.3:p.Pro373Ser
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1246C>T
  hgvsp: ENSP00000316779.5:p.Pro416Ser
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2196C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2196C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3053C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1077C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2196C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2527C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1077C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2196C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1077C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2196C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2527C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro416Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

2-127811016-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811016
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811016
    reference: chr 2
allele count: 1
allele frequency: 8.594461728861921e-6
allele num: 116354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2528T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2197T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1116T>A
  hgvsp: ENST00000357970.3:c.1116T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2197T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2197T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1078T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2528T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1078T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2197T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3052T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1245T>A
  hgvsp: ENST00000316724.5:c.1245T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2197T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2197T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1078T>A
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile415Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/2-127811021-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811021
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811021
    reference: chr 2
allele count: 4
allele frequency: 3.444415740979936e-5
allele num: 116130
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2202T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111T>G
  hgvsp: ENSP00000350654.3:p.Ser371Ala
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240T>G
  hgvsp: ENSP00000316779.5:p.Ser414Ala
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3047T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1083T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2202T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2202T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2533T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2202T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2533T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2202T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2202T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1083T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1083T>G
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15097
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19410
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser414Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

2-127811026-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811026
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811026
    reference: chr 2
allele count: 1
allele frequency: 8.634832915983076e-6
allele num: 115810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1088C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1088C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2207C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-5C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3042C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2207C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2207C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-5C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2207C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2538C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2207C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2538C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1088C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2207C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18305
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1240-5C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum

http://identifiers.org/exac.variant/2-127811027-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811027
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811027
    reference: chr 2
allele count: 1
allele frequency: 8.642444774777888e-6
allele num: 115708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2208G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1089G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2208G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-6G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2539G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1089G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1089G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3041G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2208G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2208G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2539G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-6G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2208G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2208G>T
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14861
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1240-6G>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

2-127811027-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811027
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811027
    reference: chr 2
allele count: 6
allele frequency: 5.185466864866733e-5
allele num: 115708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2208G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2208G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3041G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-6G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2539G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2208G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2208G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2208G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1089G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2539G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-6G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1089G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2208G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1089G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18251
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1240-6G>A
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

2-127811028-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811028
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811028
    reference: chr 2
allele count: 1
allele frequency: 8.660258075690655e-6
allele num: 115470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2209C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-7C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1090C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3040C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2209C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-7C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2209C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2209C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2540C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1090C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2209C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2209C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1090C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2540C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14801
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1240-7C>T
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-127811038-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811038
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811038
    reference: chr 2
allele count: 4
allele frequency: 3.479713271626418e-5
allele num: 114952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2219C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2219C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1100C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2550C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2219C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3030C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2219C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1100C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1100C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-17C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-17C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2219C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2550C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2219C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15510
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

2-127811038-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811038
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811038
    reference: chr 2
allele count: 1
allele frequency: 8.699283179066045e-6
allele num: 114952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1100C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2219C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2219C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-17C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-17C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1100C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2219C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1100C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3030C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2219C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2550C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2219C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2219C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2550C>G
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15510
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

2-127811040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811040
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811040
    reference: chr 2
allele count: 4
allele frequency: 3.481227480809734e-5
allele num: 114902
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-19C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2221C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2552C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1102C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2221C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1102C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2221C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2552C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3028C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2221C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2221C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1102C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2221C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-19C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

2-127811041-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811041
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811041
    reference: chr 2
allele count: 1
allele frequency: 8.718243796969539e-6
allele num: 114702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2222G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2222G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1103G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2222G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3027G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2222G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2222G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1103G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-20G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-20G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1103G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2222G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2553G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2553G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

2-127811042-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811042
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811042
    reference: chr 2
allele count: 14633
allele frequency: 1.277076678710443e-1
allele num: 114582
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3026C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1104C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2223C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1104C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2223C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2223C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2223C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-21C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2223C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2554C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1104C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-21C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2223C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2554C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13052
  bin: 2.25e1
  variant carriers: 2294
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 972
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.5e0
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 1.75e1
  variant carriers: 1983
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 8.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.75e1
  variant carriers: 336
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 12776
  bin: 2.75e1
  variant carriers: 2005
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 3.25e1
  variant carriers: 1510
genotype depth: GenotypeDepth
  all individuals: 9481
  bin: 1.25e1
  variant carriers: 997
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.25e1
  variant carriers: 181
genotype quality: GenotypeQuality
num of homozygotes: 1009
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP

2-127811048-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811048
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811048
    reference: chr 2
allele count: 1
allele frequency: 8.84830466482622e-6
allele num: 113016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3020C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1110C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2229C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-27C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1110C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-27C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2229C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2229C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2229C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1110C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2560C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2229C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2560C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2229C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5709
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10889
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

2-127811049-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811049
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811049
    reference: chr 2
allele count: 39
allele frequency: 3.45855060125572e-4
allele num: 112764
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-28T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2561T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3019T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2230T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2230T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2230T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1111T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-28T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1111T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2230T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2230T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2561T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2230T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1111T>C
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9415
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7446
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13971
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11452
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

2-127811051-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811051
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811051
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 112686
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1113T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3017T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2563T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2232T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-30T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-30T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2232T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2232T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1113T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2563T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2232T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1113T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2232T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2232T>C
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP

2-127811059-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811059
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811059
    reference: chr 2
allele count: 1
allele frequency: 8.949186518945427e-6
allele num: 111742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3009G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2240G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-38G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1121G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2240G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2571G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2240G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-38G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1121G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2240G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1121G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2240G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2240G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2571G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14610
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP

2-127811063-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811063
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811063
    reference: chr 2
allele count: 1
allele frequency: 9.002682799474243e-6
allele num: 111078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3005C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1125C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2244C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-42C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2244C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1125C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2575C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1125C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2575C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2244C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2244C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-42C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2244C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2244C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14411
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

2-127811068-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811068
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811068
    reference: chr 2
allele count: 1
allele frequency: 9.223900972199163e-6
allele num: 108414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2580C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2580C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1130C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2249C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-47C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-47C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2249C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1130C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1130C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.3000C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2249C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2249C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2249C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2249C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14263
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-127811071-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811071
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811071
    reference: chr 2
allele count: 1
allele frequency: 9.306134603930912e-6
allele num: 107456
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1133T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-50T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2252T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2252T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2252T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2252T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-50T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2583T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2997T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2583T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2252T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1133T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2252T>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1133T>A
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13734
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4809
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

2-127811073-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811073
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811072
    reference: chr 2
allele count: 2
allele frequency: 1.880936706479827e-5
allele num: 106330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2255delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2255delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1240-53delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2586delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2255delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2255delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2255delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2255delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1136delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1136delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2994delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1111-53delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1136delC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2586delC
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14167
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: AG
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

2-127811431-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811431
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811431
    reference: chr 2
allele count: 227
allele frequency: 1.184018360108492e-2
allele num: 19172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1110+50A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2612A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1493A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1493A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2943A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2637A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2612A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2612A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1493A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2612A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2612A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1239+50A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2943A>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2612A>C
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 1.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 1.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 27168
  bin: 2.5e0
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 7.5e0
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 2.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
num of homozygotes: 12
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

2-127811435-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811435
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811435
    reference: chr 2
allele count: 1
allele frequency: 5.220296512841929e-5
allele num: 19156
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2616G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1239+46G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2633G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1497G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1497G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2616G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1497G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2947G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1110+46G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2616G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2616G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2947G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2616G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2616G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

2-127811441-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811441
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811441
    reference: chr 2
allele count: 1
allele frequency: 5.225206395652628e-5
allele num: 19138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1503C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2622C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2627C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2622C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1503C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2953C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2622C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1503C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2953C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1110+40C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1239+40C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2622C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2622C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2622C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

2-127811465-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811465
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811465
    reference: chr 2
allele count: 2
allele frequency: 1.031140441328109e-4
allele num: 19396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-2977C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2603C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2646C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2646C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1110+16C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1527C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1239+16C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2646C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-2977C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2646C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2646C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2646C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1527C>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1527C>G
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

2-127811493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811493
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811493
    reference: chr 2
allele count: 2
allele frequency: 1.01347927434884e-4
allele num: 19734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2674G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1555G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2674G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1098G>A
  hgvsp: ENST00000357970.3:c.1098G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2575G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3005G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2674G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2674G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2674G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1227G>A
  hgvsp: ENST00000316724.5:c.1227G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2674G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1555G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3005G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1555G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33384
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr409Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

2-127811494-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811494
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811494
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 19768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1556C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1226C>T
  hgvsp: ENSP00000316779.5:p.Thr409Met
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3006C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2574C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2675C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2675C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2675C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2675C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2675C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1556C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3006C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1097C>T
  hgvsp: ENSP00000350654.3:p.Thr366Met
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1556C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2675C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33527
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr409Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

2-127811502-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811502
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811502
    reference: chr 2
allele count: 1
allele frequency: 5.023610971566362e-5
allele num: 19906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2683G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3014G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2683G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2683G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2566G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2683G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3014G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1564G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1218G>A
  hgvsp: ENST00000316724.5:c.1218G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1089G>A
  hgvsp: ENST00000357970.3:c.1089G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2683G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1564G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2683G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1564G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33939
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys406Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

2-127811515-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811515
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811515
    reference: chr 2
allele count: 2
allele frequency: 1.0e-4
allele num: 20000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3027C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1076C>T
  hgvsp: ENSP00000350654.3:p.Thr359Met
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1577C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2696C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2553C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2696C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1577C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1577C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2696C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2696C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3027C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2696C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1205C>T
  hgvsp: ENSP00000316779.5:p.Thr402Met
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2696C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr402Met
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

2-127811522-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811522
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811522
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 20084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1584C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2546C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2703C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1584C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1198C>A
  hgvsp: ENSP00000316779.5:p.Pro400Thr
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1069C>A
  hgvsp: ENSP00000350654.3:p.Pro357Thr
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2703C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3034C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3034C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1584C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2703C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2703C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2703C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2703C>A
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34410
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro400Thr
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

2-127811523-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811523
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811523
    reference: chr 2
allele count: 2
allele frequency: 9.962143853357243e-5
allele num: 20076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1585G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2704G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3035G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1068G>A
  hgvsp: ENST00000357970.3:c.1068G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2545G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2704G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1197G>A
  hgvsp: ENST00000316724.5:c.1197G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1585G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3035G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2704G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1585G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2704G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2704G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2704G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro399Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

2-127811557-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811557
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811557
    reference: chr 2
allele count: 1
allele frequency: 4.934372841211882e-5
allele num: 20266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2738C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2738C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1034C>T
  hgvsp: ENSP00000350654.3:p.Ala345Val
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2511C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1619C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1619C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1163C>T
  hgvsp: ENSP00000316779.5:p.Ala388Val
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2738C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2738C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2738C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3069C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3069C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2738C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1619C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33053
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala388Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-127811577-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811577
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811577
    reference: chr 2
allele count: 1
allele frequency: 5.007009813739235e-5
allele num: 19972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2758G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1639G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2491G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2758G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1143G>A
  hgvsp: ENST00000316724.5:c.1143G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2758G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3089G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3089G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1014G>A
  hgvsp: ENST00000357970.3:c.1014G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2758G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1639G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2758G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1639G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2758G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30980
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro381Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

2-127811582-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811582
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811582
    reference: chr 2
allele count: 2
allele frequency: 1.003310926055985e-4
allele num: 19934
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1009G>A
  hgvsp: ENSP00000350654.3:p.Ala337Thr
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1138G>A
  hgvsp: ENSP00000316779.5:p.Ala380Thr
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2763G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2763G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2486G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2763G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2763G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3094G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1644G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2763G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1644G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1644G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2763G>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3094G>A
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30557
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala380Thr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

2-127811591-T-TGGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811591
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811594
    reference: chr 2
allele count: 3
allele frequency: 1.518064973180852e-4
allele num: 19762
alternate allele: TGGC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2775_557-2773dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1656_1039-1654dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3106_910-3104dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2775_955-2773dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2775_1084-2773dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1003-6_1003-4dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1132-6_1132-4dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1656_1003-1654dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2775_546-2773dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3106_955-3104dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2775_1039-2773dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1656_910-1654dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2474_2476dupGCC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2775_910-2773dupGCC
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29380
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.1132-6_1132-4dupGCC
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

2-127811592-G-GGCAGCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811592
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811598
    reference: chr 2
allele count: 1
allele frequency: 5.083884087442806e-5
allele num: 19670
alternate allele: GGCAGCA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1132-10_1132-5dupTGCTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2470_2475dupTGCTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1003-10_1003-5dupTGCTGC
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28912
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1132-10_1132-5dupTGCTGC
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-127811592-GGCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811592
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811589
    reference: chr 2
allele count: 2
allele frequency: 1.016776817488561e-4
allele num: 19670
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2473_2475delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1657_910-1655delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2776_557-2774delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1132-7_1132-5delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1003-7_1003-5delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2776_1084-2774delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3107_910-3105delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2776_546-2774delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1657_1039-1655delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2776_955-2774delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3107_955-3105delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1657_1003-1655delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2776_910-2774delTGC
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2776_1039-2774delTGC
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 28912
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1132-7_1132-5delTGC
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: GGCA
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

2-127811595-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811595
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811595
    reference: chr 2
allele count: 47
allele frequency: 2.432460407825277e-3
allele num: 19322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1657T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1003-7T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1657T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2776T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2776T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1657T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2776T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2776T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3107T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2473T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1132-7T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2776T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2776T>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3107T>C
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27446
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: c.1132-7T>C
num of homozygotes: 1
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

2-127811613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811613
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811613
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 19642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1675C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1003-25C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2455C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2794C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2794C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2794C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2794C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2794C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2794C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1675C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3125C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1132-25C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3125C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1675C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28149
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

2-127811614-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811614
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811614
    reference: chr 2
allele count: 1
allele frequency: 5.094762584063582e-5
allele num: 19628
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2795C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2795C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1132-26C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1676C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2795C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2454C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2795C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2795C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1676C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1676C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2795C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3126C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1003-26C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3126C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-127811617-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811617
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811617
    reference: chr 2
allele count: 1
allele frequency: 5.103603143819537e-5
allele num: 19594
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2451C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1679C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2798C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1132-29C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2798C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1679C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2798C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1003-29C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2798C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2798C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3129C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1679C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2798C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3129C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28018
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-127811621-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811621
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811621
    reference: chr 2
allele count: 1
allele frequency: 5.103082261686059e-5
allele num: 19596
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1003-33G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1683G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2802G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3133G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2802G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2802G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2802G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2802G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2802G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1683G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2447G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1132-33G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3133G>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1683G>T
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/2-127811640-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127811640
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127811640
    reference: chr 2
allele count: 1
allele frequency: 5.091649694501019e-5
allele num: 19640
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.955-2821T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.546-2821T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.910-3152T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1003-1702T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1003-52T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.910-1702T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000462958
  gene symbol: BIN1
  hgvsc: ENST00000462958.1:n.2428T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1039-2821T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1132-52T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.955-3152T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.557-2821T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1084-2821T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1039-1702T>G
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.910-2821T>G
  variant of: http://identifiers.org/hgnc/1052
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28750
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

2-127815019-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127815019
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127815019
    reference: chr 2
allele count: 2
allele frequency: 1.147446930579461e-4
allele num: 17430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.556+30C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.954+1568C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.545+1568C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1002+1568C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1002+1568C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.909+1568C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1083+30C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1131+30C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.954+1568C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.909+1568C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1038+30C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.909+1568C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1038+30C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34408
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

2-127815022-AGCTGGGCCGCGGCGGCCGCG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127815022
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127815002
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 17368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34276
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1131+7_1131+26delCGCGGCCGCCGCGGCCCAGC
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: AGCTGGGCCGCGGCGGCCGCG
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

2-127815023-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127815023
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127815023
    reference: chr 2
allele count: 1
allele frequency: 5.759705103098721e-5
allele num: 17362
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1131+26C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.909+1564C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1038+26C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.909+1564C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1083+26C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.909+1564C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.954+1564C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1038+26C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.556+26C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1002+1564C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.545+1564C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.954+1564C>A
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1002+1564C>A
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

2-127815024-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127815024
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127815024
    reference: chr 2
allele count: 1
allele frequency: 5.769674590353104e-5
allele num: 17332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  hgvsc: ENST00000357970.3:c.1002+1563G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.545+1563G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  hgvsc: ENST00000409400.1:c.909+1563G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  hgvsc: ENST00000484253.1:n.556+25G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1038+25G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1083+25G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  hgvsc: ENST00000376113.2:c.954+1563G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  hgvsc: ENST00000393041.3:c.909+1563G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  hgvsc: ENST00000351659.3:c.1002+1563G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.954+1563G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.909+1563G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  hgvsc: ENST00000346226.3:c.1038+25G>C
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1131+25G>C
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

2-127815026-GGGCCGCGGC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127815026
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127815017
    reference: chr 2
allele count: 1
allele frequency: 5.74184657785944e-5
allele num: 17416
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000365281
  ensembl transcript: ENST00000376113
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000350654
  ensembl transcript: ENST00000357970
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315411
  ensembl transcript: ENST00000346226
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315388
  ensembl transcript: ENST00000351659
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000484253
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000386797
  ensembl transcript: ENST00000409400
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376761
  ensembl transcript: ENST00000393041
  gene symbol: BIN1
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33824
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: GGGCCGCGGC
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

2-127815031-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 127815031
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 127815031
    reference: chr 2
allele count: 26
allele frequency: 1.484187692658979e-3
allele num: 17518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259238
  ensembl transcript: ENST00000259238
  gene symbol: BIN1
  hgvsc: ENST00000259238.4:c.1083+18C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000376760
  ensembl transcript: ENST00000393040
  gene symbol: BIN1
  hgvsc: ENST00000393040.3:c.1038+18C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000315284
  ensembl transcript: ENST00000352848
  gene symbol: BIN1
  hgvsc: ENST00000352848.3:c.954+1556C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000316779
  ensembl transcript: ENST00000316724
  gene symbol: BIN1
  hgvsc: ENST00000316724.5:c.1131+18C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl transcript: ENST00000466111
  gene symbol: BIN1
  hgvsc: ENST00000466111.1:n.545+1556C>T
  variant of: http://identifiers.org/hgnc/1052
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136717
  ensembl protein: ENSP00000259237
  ensembl transcript: ENST00000348750
  gene symbol: BIN1
  hgvsc: ENST00000348750.4:c.909+1556C>T
  variant of: http://identifiers.org/hgnc/1052
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 812
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12013
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5327
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27696
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2283
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 562
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1004
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 3.92756e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.64e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.625e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.23e0

GenotypeDepth
all individuals: 204
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3058
bin: 1.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 5426
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26373
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 828
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4345
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6294
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7992
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5774
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 4.012841091492777e-4
allele num: 7476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 3.68347e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.98e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

FS
type: SiteQuality
SIO_000300: 5.546e0

VQSLOD
type: SiteQuality
SIO_000300: -1.546e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

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

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

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5426
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6294
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 513
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4345
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7992
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 26373
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 188
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 211
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5774
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 5.546e0

VQSLOD
type: SiteQuality
SIO_000300: -1.546e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.98e-2

DP
type: SiteQuality
SIO_000300: 3.68347e5

GenotypeDepth
all individuals: 1095
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6709
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6342
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25483
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5172
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6711
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.364628820960699e-4
allele num: 7328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 5.383e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.05e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.873e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.53493e5

QD
type: SiteQuality
SIO_000300: 1.467e1

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6709
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6342
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5172
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25483
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6711
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 833
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.896094046264695e-4
allele num: 5274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.05e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 5.383e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

QD
type: SiteQuality
SIO_000300: 1.467e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.873e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 3.53493e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 2
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 405
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25459
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6764
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 980
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6815
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5026
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6358
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 104
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.53209e5

VQSLOD
type: SiteQuality
SIO_000300: 1.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.21e-2

QD
type: SiteQuality
SIO_000300: 9.94e0

MQ
type: SiteQuality
SIO_000300: 5.805e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.134e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.36e-1

GenotypeDepth
all individuals: 427
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 481
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 390
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 464
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 383
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1776
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17720
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3585
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2572
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1751
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3290
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2830
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4999
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1086
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10282
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3494
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 7.5e0
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6042
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.383222116301239e-4
allele num: 8392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15918
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64138
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11176
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.616e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.101e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.95e-1

FS
type: SiteQuality
SIO_000300: 1.182e0

DP
type: SiteQuality
SIO_000300: 2.099829e6

QD
type: SiteQuality
SIO_000300: 7.83e0

GenotypeDepth
all individuals: 527
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5128
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12768
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 480
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 390
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3673
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1771
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3190
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19078
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1858
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3267
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2811
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2557
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5021
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10280
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1652
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11184
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.02757502027575e-4
allele num: 9864
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.280618012812461e-5
allele num: 15922
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64130
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

QD
type: SiteQuality
SIO_000300: 1.031e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.101026e6

GenotypeDepth
all individuals: 1636
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 527
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 390
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 480
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19774
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10278
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2515
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1705
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2922
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3714
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5055
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2805
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1753
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1833
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3213
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1643
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.187366421277606e-4
allele num: 8422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.111968631356196e-5
allele num: 64268
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15940
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: 6052
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -8.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

MQRankSum
type: SiteQuality
SIO_000300: -7.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.101282e6

QD
type: SiteQuality
SIO_000300: 1.453e1

GenotypeDepth
all individuals: 794
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 527
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4548
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8467
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 464
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3790
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10276
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2514
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21137
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2782
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1672
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5088
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6066
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.67379679144385e-4
allele num: 11220
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64294
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.103851e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

QD
type: SiteQuality
SIO_000300: 1.325e1

VQSLOD
type: SiteQuality
SIO_000300: 8.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

GenotypeDepth
all individuals: 464
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5130
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 526
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16249
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 539
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2578
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23294
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2781
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4822
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1535
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1783
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3861
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10262
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1664
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2301
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6032
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9866
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15928
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558117793705204e-5
allele num: 64180
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

FS
type: SiteQuality
SIO_000300: 1.402e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.113226e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.997e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.76e-1

QD
type: SiteQuality
SIO_000300: 1.063e1

MQ
type: SiteQuality
SIO_000300: 5.879e1

GenotypeDepth
all individuals: 526
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 801
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 480
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1786
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2594
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1597
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3865
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1520
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22716
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10261
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2786
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.512562814070352e-4
allele num: 15920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6024
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64142
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11194
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.791e0

MQRankSum
type: SiteQuality
SIO_000300: -4.53e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.393e1

FS
type: SiteQuality
SIO_000300: 2.661e0

DP
type: SiteQuality
SIO_000300: 2.114688e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

GenotypeDepth
all individuals: 1570
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 412
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 479
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2119
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4455
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 214
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25336
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1251
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1663
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10219
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 313
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3761
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4659
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1546
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1612
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.711351215528614e-5
allele num: 63676
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.029654036243822e-4
allele num: 9712
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5776
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15916
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11172
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.968e1

DP
type: SiteQuality
SIO_000300: 2.12227e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.996e0

MQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 7.5023e1

QD
type: SiteQuality
SIO_000300: 2.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.659e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e0

GenotypeDepth
all individuals: 4321
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 410
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 481
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 476
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 435
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 161
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10266
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 337
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1643
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3851
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1532
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4850
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26973
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1050
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.221807435059884e-5
allele num: 64290
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11208
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.013171225937183e-4
allele num: 9870
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: 6048
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.074e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 1.911e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

DP
type: SiteQuality
SIO_000300: 2.126305e6

GenotypeDepth
all individuals: 5128
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 476
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 523
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 537
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1535
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3816
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10269
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 749
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4923
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 944
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28888
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64362
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.183992422448496e-4
allele num: 8446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15972
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.928571428571429e-5
allele num: 11200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6062
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.146389e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

QD
type: SiteQuality
SIO_000300: 1.222e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

GenotypeDepth
all individuals: 523
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 378
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4451
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 435
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1538
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4914
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10273
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1135
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3794
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30083
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6060
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.355230274901821e-4
allele num: 11204
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.011736139214893e-4
allele num: 9884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15962
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.987e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.889999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.5e-2

QD
type: SiteQuality
SIO_000300: 1.011e1

DP
type: SiteQuality
SIO_000300: 2.153266e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.45e-1

GenotypeDepth
all individuals: 403
bin: 6.25e1
variant carriers: 14

GenotypeDepth
all individuals: 474
bin: 7.75e1
variant carriers: 4

GenotypeDepth
all individuals: 433
bin: 7.25e1
variant carriers: 9

GenotypeDepth
all individuals: 522
bin: 9.25e1
variant carriers: 3

GenotypeDepth
all individuals: 5159
bin: 9.75e1
variant carriers: 58

GenotypeQuality
all individuals: 460
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3744
bin: 2.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1265
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1554
bin: 7.75e1
variant carriers: 6

GenotypeQuality
all individuals: 479
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1574
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1474
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1069
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29797
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 11151
bin: 9.75e1
variant carriers: 1055

GenotypeQuality
all individuals: 735
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 76
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 460
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 595
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 895
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 370
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 4813
bin: 6.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 890
allele frequency: 1.381429857510943e-2
allele num: 64426
num of homozygotes: 7

Other
type: Population
allele count: 3
allele frequency: 3.529411764705882e-3
allele num: 850
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.365744026496333e-4
allele num: 8454
num of homozygotes: 0

Latino
type: Population
allele count: 22
allele frequency: 1.963935011605071e-3
allele num: 11202
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 115
allele frequency: 1.898316275998679e-2
allele num: 6058
num of homozygotes: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15956
num of homozygotes: 0

African
type: Population
allele count: 64
allele frequency: 6.472491909385114e-3
allele num: 9888
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

QD
type: SiteQuality
SIO_000300: 1.221e1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.16448e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

GenotypeDepth
all individuals: 428
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5154
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 472
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 536
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4472
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 525
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3838
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30919
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4938
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10201
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 99
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1586
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.261740763932373e-5
allele num: 15970
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6066
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64426
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.501e0

DP
type: SiteQuality
SIO_000300: 2.159205e6

QD
type: SiteQuality
SIO_000300: 2.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.24e-1

FS
type: SiteQuality
SIO_000300: 4.971e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.217e0

GenotypeDepth
all individuals: 15199
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4537
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1961
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 394
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5154
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4578
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1537
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4765
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10194
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30511
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5994
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.962179602079225e-5
allele num: 11158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64166
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15890
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

FS
type: SiteQuality
SIO_000300: 8.465e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.06e-1

DP
type: SiteQuality
SIO_000300: 2.157231e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.179e-1

GenotypeDepth
all individuals: 20292
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 15213
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 408
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 731
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 525
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10194
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 869
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4584
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30914
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1238
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1421
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4771
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.557777985481509e-5
allele num: 64194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5990
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.360000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.454e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

DP
type: SiteQuality
SIO_000300: 2.156994e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.581e0

QD
type: SiteQuality
SIO_000300: 1.646e1

MQRankSum
type: SiteQuality
SIO_000300: -1.517e0

GenotypeDepth
all individuals: 394
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 525
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 476
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 536
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 472
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 408
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29881
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10196
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1024
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5031
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4719
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1525
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64106
num of homozygotes: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.780114722753346e-4
allele num: 8368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5964
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.147499e6

FS
type: SiteQuality
SIO_000300: 2.515e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.77e-1

QD
type: SiteQuality
SIO_000300: 1.175e1

GenotypeDepth
all individuals: 369
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 476
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1497
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5154
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14840
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 472
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5651
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4600
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1788
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10192
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1552
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1510
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 106
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28318
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564112991522508e-5
allele num: 63934
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5950
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15794
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.134008e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.04e-1

QD
type: SiteQuality
SIO_000300: 6.88e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.166e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

GenotypeDepth
all individuals: 394
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2637
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 428
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 733
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 536
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18251
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 131
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4544
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1488
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5666
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10199
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 28491
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9826
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63866
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.996041741633681e-5
allele num: 11116
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.73e-1

DP
type: SiteQuality
SIO_000300: 2.134538e6

QD
type: SiteQuality
SIO_000300: 1.013e1

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

FS
type: SiteQuality
SIO_000300: 1.903e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.8e-1

GenotypeDepth
all individuals: 5154
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14861
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 1497
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4493
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 536
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 525
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1488
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28491
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5666
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 103
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10199
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 4544
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.334726973267453e-5
allele num: 15786
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.828891742084991e-5
allele num: 63866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11116
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.013e1

FS
type: SiteQuality
SIO_000300: 1.903e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

MQRankSum
type: SiteQuality
SIO_000300: -2.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.26e-1

DP
type: SiteQuality
SIO_000300: 2.134538e6

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 9.73e-1

GenotypeDepth
all individuals: 111
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 369
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 394
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 525
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 476
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1511
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1357
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4440
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10190
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 139
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27433
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5901
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1911
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9824
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11092
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.352432981832041e-5
allele num: 15742
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.57e0

VQSLOD
type: SiteQuality
SIO_000300: -1.179e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

DP
type: SiteQuality
SIO_000300: 2.130007e6

MQRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.94e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

GenotypeDepth
all individuals: 369
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 394
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 525
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 536
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2647
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7424
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23892
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1740
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10192
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2215
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11044
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 5.091649694501018e-4
allele num: 5892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15694
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.575497857322914e-5
allele num: 63472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

FS
type: SiteQuality
SIO_000300: 3.707e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.473e0

DP
type: SiteQuality
SIO_000300: 2.090542e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.48e-1

QD
type: SiteQuality
SIO_000300: 1.157e1

GenotypeDepth
all individuals: 428
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 476
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4351
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 472
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 369
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23892
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2647
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7424
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2215
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1740
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10192
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63472
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.214181641573579e-4
allele num: 8236
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11044
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.707e0

QD
type: SiteQuality
SIO_000300: 1.157e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.473e0

VQSLOD
type: SiteQuality
SIO_000300: 8.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

DP
type: SiteQuality
SIO_000300: 2.090542e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 536
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 525
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4316
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 472
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 408
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4083
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23689
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1780
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10187
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1119
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2265
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7608
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2756
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1323
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63444
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11044
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8248
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.549719530851606e-4
allele num: 15688
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.085827e6

QD
type: SiteQuality
SIO_000300: 1.051e1

MQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.54e0

FS
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.27e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

GenotypeDepth
all individuals: 362
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 394
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1478
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 525
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 536
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2860
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4041
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10187
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 628
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7723
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2336
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23173
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1300
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11030
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.579030475288173e-5
allele num: 63330
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.506e1

DP
type: SiteQuality
SIO_000300: 2.080868e6

MQRankSum
type: SiteQuality
SIO_000300: 5.26e-1

FS
type: SiteQuality
SIO_000300: 2.886e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.57e-1

GenotypeDepth
all individuals: 419
bin: 9.25e1
variant carriers: 38

GenotypeDepth
all individuals: 954
bin: 4.25e1
variant carriers: 571

GenotypeDepth
all individuals: 6154
bin: 9.75e1
variant carriers: 2403

GenotypeDepth
all individuals: 407
bin: 8.75e1
variant carriers: 33

GenotypeDepth
all individuals: 369
bin: 7.75e1
variant carriers: 41

GenotypeQuality
all individuals: 19374
bin: 6.25e1
variant carriers: 91

GenotypeQuality
all individuals: 443
bin: 4.75e1
variant carriers: 80

GenotypeQuality
all individuals: 19684
bin: 9.75e1
variant carriers: 12773

GenotypeQuality
all individuals: 132
bin: 1.25e1
variant carriers: 21

GenotypeQuality
all individuals: 2611
bin: 3.25e1
variant carriers: 48

GenotypeQuality
all individuals: 278
bin: 9.25e1
variant carriers: 69

GenotypeQuality
all individuals: 481
bin: 5.25e1
variant carriers: 87

GenotypeQuality
all individuals: 209
bin: 2.5e0
variant carriers: 10

GenotypeQuality
all individuals: 169
bin: 1.75e1
variant carriers: 25

GenotypeQuality
all individuals: 745
bin: 7.25e1
variant carriers: 64

GenotypeQuality
all individuals: 1406
bin: 3.75e1
variant carriers: 68

GenotypeQuality
all individuals: 534
bin: 5.75e1
variant carriers: 46

GenotypeQuality
all individuals: 491
bin: 8.25e1
variant carriers: 97

GenotypeQuality
all individuals: 2159
bin: 2.75e1
variant carriers: 32

GenotypeQuality
all individuals: 244
bin: 7.5e0
variant carriers: 17

GenotypeQuality
all individuals: 7375
bin: 2.25e1
variant carriers: 31

GenotypeQuality
all individuals: 216
bin: 8.75e1
variant carriers: 58

GenotypeQuality
all individuals: 2873
bin: 6.75e1
variant carriers: 83

GenotypeQuality
all individuals: 461
bin: 4.25e1
variant carriers: 52

GenotypeQuality
all individuals: 808
bin: 7.75e1
variant carriers: 107

Other
type: Population
allele count: 136
allele frequency: 1.630695443645084e-1
allele num: 834
num of homozygotes: 12

Latino
type: Population
allele count: 709
allele frequency: 6.452493629413907e-2
allele num: 10988
num of homozygotes: 29

African
type: Population
allele count: 1738
allele frequency: 1.778915046059365e-1
allele num: 9770
num of homozygotes: 128

East Asian
type: Population
allele count: 127
allele frequency: 1.55029296875e-2
allele num: 8192
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 8051
allele frequency: 1.273569982282966e-1
allele num: 63216
num of homozygotes: 485

European (Finnish)
type: Population
allele count: 779
allele frequency: 1.329351535836177e-1
allele num: 5860
num of homozygotes: 57

South Asian
type: Population
allele count: 3093
allele frequency: 1.967306958402239e-1
allele num: 15722
num of homozygotes: 297

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.408e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.66e-1

FS
type: SiteQuality
SIO_000300: 1.195e0

QD
type: SiteQuality
SIO_000300: 1.396e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.47e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.89e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 2.288935e6

GenotypeDepth
all individuals: 406
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 365
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3573
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 272
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9606
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 192
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4571
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3443
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21360
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10764
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3433
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.602307322544464e-5
allele num: 62410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10914
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5744
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.628e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.281e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e-1

DP
type: SiteQuality
SIO_000300: 2.042115e6

MQ
type: SiteQuality
SIO_000300: 5.903e1

QD
type: SiteQuality
SIO_000300: 3.33e0

GenotypeDepth
all individuals: 272
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 440
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 503
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3425
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 5368
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2972
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3806
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3141
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11071
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9634
bin: 9.75e1
variant carriers: 40

GenotypeQuality
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18099
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 38
allele frequency: 3.994953742640875e-3
allele num: 9512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8168
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.175995595522114e-5
allele num: 10898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5718
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.53e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 1.929e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

DP
type: SiteQuality
SIO_000300: 2.016225e6

QD
type: SiteQuality
SIO_000300: 1.405e1

GenotypeDepth
all individuals: 407
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9548
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 490
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5711
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19019
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3811
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 609
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5352
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11243
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2938
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9603
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3105
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8156
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62254
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

MQ
type: SiteQuality
SIO_000300: 5.705e1

VQSLOD
type: SiteQuality
SIO_000300: -1.068e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

QD
type: SiteQuality
SIO_000300: 1.364e1

MQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

DP
type: SiteQuality
SIO_000300: 2.01381e6

GenotypeDepth
all individuals: 407
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2983
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5711
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 502
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 11529
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4408
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4998
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13488
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9600
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 183
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6948
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2549
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9412
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.591957811470006e-5
allele num: 15170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.359999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.609e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.501e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.96019e6

GenotypeDepth
all individuals: 7180
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5711
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14472
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11324
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5991
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2184
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9601
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2036
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4583
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10734
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7386
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8052
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10794
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.627922120205769e-5
allele num: 61428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

FS
type: SiteQuality
SIO_000300: 3.214e0

DP
type: SiteQuality
SIO_000300: 1.936745e6

QD
type: SiteQuality
SIO_000300: 2.869e1

VQSLOD
type: SiteQuality
SIO_000300: -3.031e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.437e0

MQRankSum
type: SiteQuality
SIO_000300: -5.78e-1

GenotypeDepth
all individuals: 418
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 433
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 502
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8919
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4172
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5114
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9600
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7632
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2896
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1948
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4575
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6889
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9546
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60074
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9086
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14746
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.276487107480215e-4
allele num: 7834
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10566
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.881e0

DP
type: SiteQuality
SIO_000300: 1.912794e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.45e-1

QD
type: SiteQuality
SIO_000300: 8.289999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.353e0

GenotypeDepth
all individuals: 316
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5711
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 272
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 490
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4567
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2949
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7640
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9600
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8908
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4528
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6923
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2930
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2536
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.821282401091406e-5
allele num: 14660
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7746
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9026
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.909138e6

QD
type: SiteQuality
SIO_000300: 5.04e0

VQSLOD
type: SiteQuality
SIO_000300: -1.737e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

GenotypeDepth
all individuals: 316
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5711
bin: 9.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 365
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8188
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2951
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4532
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7612
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1174
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6910
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4566
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3379
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 986
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9600
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2788
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3268
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1397
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.122082585278277e-4
allele num: 8912
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.696870969931446e-5
allele num: 58932
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14566
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

QD
type: SiteQuality
SIO_000300: 1.505e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 1.9091e6

FS
type: SiteQuality
SIO_000300: 5.227e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

GenotypeDepth
all individuals: 40
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 7.75e1
variant carriers: 3

GenotypeDepth
all individuals: 340
bin: 5.25e1
variant carriers: 8

GenotypeDepth
all individuals: 66
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 47
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 362
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 439
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 573
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 10552
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 299
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 130
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 959
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 693
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 486
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3438
bin: 9.75e1
variant carriers: 210

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 241
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 219
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 271
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 16323
bin: 7.5e0
variant carriers: 17

GenotypeQuality
all individuals: 615
bin: 1.25e1
variant carriers: 6

GenotypeQuality
all individuals: 627
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 488
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 248
bin: 5.25e1
variant carriers: 6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

African
type: Population
allele count: 221
allele frequency: 9.185369908561929e-2
allele num: 2406
num of homozygotes: 12

South Asian
type: Population
allele count: 1
allele frequency: 1.277139208173691e-4
allele num: 7830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 3.887017362010883e-4
allele num: 7718
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 5.154639175257732e-3
allele num: 388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.05178e5

VQSLOD
type: SiteQuality
SIO_000300: 4.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

QD
type: SiteQuality
SIO_000300: 1.344e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.39e-2

GenotypeDepth
all individuals: 47
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 632
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9708
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3270
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 607
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17218
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.298026998961578e-4
allele num: 7704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7826
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 1.167e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.790000000000001e-2

DP
type: SiteQuality
SIO_000300: 4.04062e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.457e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.49e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.9e-2

QD
type: SiteQuality
SIO_000300: 1.292e1

GenotypeDepth
all individuals: 524
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1199
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1253
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19339
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3281
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1051
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7786
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7672
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.274859765425803e-4
allele num: 7844
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.793e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: -1.632e0

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.65e-1

FS
type: SiteQuality
SIO_000300: 2.647e0

DP
type: SiteQuality
SIO_000300: 4.08314e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.450000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.281e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.99e-1

GenotypeDepth
all individuals: 89
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 280
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 85
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1588
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3238
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1916
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2091
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27230
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3290
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7844
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.54000508001016e-4
allele num: 7874
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 3.32e1

DP
type: SiteQuality
SIO_000300: 4.30327e5

MQ
type: SiteQuality
SIO_000300: 5.858e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.88e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.49e-1

GenotypeDepth
all individuals: 89
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1616
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1742
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 883
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3292
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 345
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2320
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3322
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 388
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30987
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.240387000744232e-4
allele num: 8062
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.266784899923993e-4
allele num: 7894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.224e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.72e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

FS
type: SiteQuality
SIO_000300: 4.069e0

DP
type: SiteQuality
SIO_000300: 4.55306e5

VQSLOD
type: SiteQuality
SIO_000300: -1.299e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

GenotypeDepth
all individuals: 85
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 194
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 883
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 338
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3424
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3291
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2219
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31292
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 514
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8078
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.231e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.383e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.5685e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 6.67e0

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1925
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 884
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3502
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3291
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2352
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31612
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2333
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8174
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.894080996884735e-4
allele num: 2568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.71e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.133e0

FS
type: SiteQuality
SIO_000300: 5.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

DP
type: SiteQuality
SIO_000300: 4.62268e5

QD
type: SiteQuality
SIO_000300: 1.428e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

GenotypeDepth
all individuals: 526
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 195
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 278
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31917
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3456
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2523
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.529724260055654e-4
allele num: 7906
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.275e1

FS
type: SiteQuality
SIO_000300: 5.951e0

DP
type: SiteQuality
SIO_000300: 4.66314e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.67e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.256e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.24e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

GenotypeDepth
all individuals: 196
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 461
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 278
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2061
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3099
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2871
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 646
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31633
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3293
bin: 9.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7910
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.4e0

DP
type: SiteQuality
SIO_000300: 4.6622e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.679999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.11e1

GenotypeDepth
all individuals: 1276
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 527
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 278
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3293
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2503
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 133
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31790
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3202
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2825
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 3.802281368821293e-4
allele num: 2630
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.264222503160556e-4
allele num: 7910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.141e1

DP
type: SiteQuality
SIO_000300: 4.67207e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.69e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.026e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.26e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

GenotypeDepth
all individuals: 48
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 278
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29965
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2687
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3278
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3293
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 513
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2069
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.263902932254803e-4
allele num: 7912
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2702
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8384
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.5806e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.870000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.07e0

FS
type: SiteQuality
SIO_000300: 2.954e0

QD
type: SiteQuality
SIO_000300: 9.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.427e0

VQSLOD
type: SiteQuality
SIO_000300: -1.695e0

MQ
type: SiteQuality
SIO_000300: 5.888e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.152e0

GenotypeDepth
all individuals: 278
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 368
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1385
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3027
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 604
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28194
bin: 7.5e0
variant carriers: 2

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

GenotypeQuality
all individuals: 85
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2057
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 494
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3293
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 7.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.219809709685289e-4
allele num: 8198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7912
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

DP
type: SiteQuality
SIO_000300: 4.40643e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.69e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

QD
type: SiteQuality
SIO_000300: 1.468e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 2279
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 855
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 89
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27788
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 274
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2039
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 7.704160246533128e-4
allele num: 2596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.683e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.79e-2

MQRankSum
type: SiteQuality
SIO_000300: -6.75e-1

FS
type: SiteQuality
SIO_000300: 1.295e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.422e0

QD
type: SiteQuality
SIO_000300: 1.174e1

DP
type: SiteQuality
SIO_000300: 4.37859e5

VQSLOD
type: SiteQuality
SIO_000300: -1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeDepth
all individuals: 1282
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1709
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26258
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3444
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 401
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3299
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 759
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1752
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.475860361475613e-4
allele num: 8078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.263902932254803e-4
allele num: 7912
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.039e0

DP
type: SiteQuality
SIO_000300: 4.31893e5

MQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

FS
type: SiteQuality
SIO_000300: 8.002000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

QD
type: SiteQuality
SIO_000300: 1.425e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.66e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

GenotypeDepth
all individuals: 66
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 530
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4154
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25251
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1566
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 319
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 619
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.996802557953637e-4
allele num: 2502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.3154e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

QD
type: SiteQuality
SIO_000300: 3.03e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 6.932e0

VQSLOD
type: SiteQuality
SIO_000300: -4.743e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.26e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

GenotypeDepth
all individuals: 1610
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2056
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 278
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1255
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 530
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 873
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4154
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1566
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 619
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 319
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25251
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 304
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.996802557953637e-4
allele num: 2502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.264542235710673e-4
allele num: 7908
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.743e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.26e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

FS
type: SiteQuality
SIO_000300: 6.932e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

DP
type: SiteQuality
SIO_000300: 4.3154e5

QD
type: SiteQuality
SIO_000300: 3.03e0

GenotypeDepth
all individuals: 351
bin: 5.25e1
variant carriers: 5

GenotypeDepth
all individuals: 51
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 121
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 610
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3316
bin: 9.75e1
variant carriers: 41

GenotypeQuality
all individuals: 278
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 702
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21789
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 269
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 381
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 157
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 594
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 508
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1537
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 6119
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 472
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1205
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.265182186234818e-4
allele num: 7904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7782
num of homozygotes: 0

African
type: Population
allele count: 46
allele frequency: 1.910299003322259e-2
allele num: 2408
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

QD
type: SiteQuality
SIO_000300: 9.359999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

FS
type: SiteQuality
SIO_000300: 2.643e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.069999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
type: SiteQuality
SIO_000300: 4.26595e5

VQSLOD
type: SiteQuality
SIO_000300: 6.6e-2

GenotypeDepth
all individuals: 275
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 440
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 338
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23948
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4240
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 721
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 1.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1734
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3297
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7982
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.93e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.76e-2

DP
type: SiteQuality
SIO_000300: 4.24656e5

GenotypeDepth
all individuals: 275
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 877
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1636
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24204
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1777
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4070
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 473
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 615
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3297
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.264222503160556e-4
allele num: 7910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.74e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.12e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.25089e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeDepth
all individuals: 1268
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1572
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23401
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4645
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3298
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 607
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1698
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 166
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2496
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.264222503160556e-4
allele num: 7910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.047e1

DP
type: SiteQuality
SIO_000300: 4.23754e5

FS
type: SiteQuality
SIO_000300: 1.431e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.665e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.829999999999999e-2

QD
type: SiteQuality
SIO_000300: 7.32e0

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeDepth
all individuals: 59
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1268
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 338
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 877
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4771
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23378
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1748
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1706
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3299
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 4.012841091492777e-4
allele num: 2492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7954
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7910
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.268e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.08e0

QD
type: SiteQuality
SIO_000300: 5.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.81e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.004e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.81e-2

DP
type: SiteQuality
SIO_000300: 4.23857e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 195
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 881
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1264
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1551
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20889
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7791
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1452
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3299
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 386
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7912
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.255020080321285e-4
allele num: 7968
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.27775e5

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

FS
type: SiteQuality
SIO_000300: 2.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.24e-1

QD
type: SiteQuality
SIO_000300: 1.083e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.838e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.35e-2

MQ
type: SiteQuality
SIO_000300: 6.033e1

VQSLOD
type: SiteQuality
SIO_000300: -1.43e0

GenotypeDepth
all individuals: 81
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 743
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4896
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1727
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2068
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 210
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30304
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3520
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1838
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 626
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 286
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.493765586034913e-4
allele num: 8020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5510
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.428e1

MQRankSum
type: SiteQuality
SIO_000300: 4.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.26e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.05283e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.98e0

GenotypeDepth
all individuals: 86
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3448
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30416
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4971
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2098
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 200
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1836
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2656
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5530
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 4.06439e5

QD
type: SiteQuality
SIO_000300: 2.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.938e-1

MQ
type: SiteQuality
SIO_000300: 4.92e1

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 1.0993e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-2

GenotypeDepth
all individuals: 338
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 389
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4871
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3613
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 282
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2046
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30124
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1836
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 159
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.805054151624549e-4
allele num: 5540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7968
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-2

MQ
type: SiteQuality
SIO_000300: 5.89e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.059e0

DP
type: SiteQuality
SIO_000300: 4.06345e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.737e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

GenotypeDepth
all individuals: 81
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 108
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1551
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5100
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3341
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30472
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1835
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.796507213363706e-4
allele num: 2634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7958
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.312e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.383e0

MQ
type: SiteQuality
SIO_000300: 5.783e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.27e-2

DP
type: SiteQuality
SIO_000300: 4.07984e5

MQRankSum
type: SiteQuality
SIO_000300: -4.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.878e0

QD
type: SiteQuality
SIO_000300: 1.614e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.44e0

GenotypeQuality
all individuals: 30024
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3580
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5014
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1525
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2148
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1835
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 279
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 159
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7982
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.80517503805175e-4
allele num: 2628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 4.09165e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-2

MQ
type: SiteQuality
SIO_000300: 5.513e1

QD
type: SiteQuality
SIO_000300: 8.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

FS
type: SiteQuality
SIO_000300: 1.716e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.236e0

MQRankSum
type: SiteQuality
SIO_000300: -1.042e0