http://identifiers.org/exac.variant/22-29669704-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669704
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669704
    reference: chr 22
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.167-26C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.127-26C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1284C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.97-26C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.530-26C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.103-26C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.103-26C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.103-26C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.103-23C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.103-26C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.103-26C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.103-23C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.103-26C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.103-26C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.103-23C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.103-26C>A
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

22-29669712-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669712
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669712
    reference: chr 22
allele count: 7317
allele frequency: 6.036829859907925e-2
allele num: 121206
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.103-15C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.103-18C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.103-18C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.97-18C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.530-18C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.103-18C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.167-18C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.103-18C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.103-15C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.103-18C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.127-18C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.103-15C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.103-18C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.103-18C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1292C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.103-18C>G
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 6.25e1
  variant carriers: 607
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9355
  bin: 3.25e1
  variant carriers: 359
genotype depth: GenotypeDepth
  all individuals: 7729
  bin: 4.25e1
  variant carriers: 632
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 5.75e1
  variant carriers: 756
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 9.75e1
  variant carriers: 813
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 8845
  bin: 3.75e1
  variant carriers: 520
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 2.25e1
  variant carriers: 82
genotype quality: GenotypeQuality
num of homozygotes: 307
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

22-29669713-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669713
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669713
    reference: chr 22
allele count: 2
allele frequency: 1.724137931034483e-5
allele num: 116000
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.103-17G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.97-17G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.530-17G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.103-17G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.103-17G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1293G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.103-17G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.103-17G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.127-17G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.103-14G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.167-17G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.103-17G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.103-14G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.103-14G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.103-17G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.103-17G>A
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-29669713-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669713
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669714
    reference: chr 22
allele count: 2141
allele frequency: 1.845689655172414e-2
allele num: 116000
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.103-8dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.167-8dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.530-8dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.127-8dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.103-8dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.103-5dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.103-8dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.103-5dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.103-5dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.103-8dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.103-8dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.103-8dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.97-8dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1302dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.103-8dupT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.103-8dupT
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 9.75e1
  variant carriers: 220
genotype depth: GenotypeDepth
  all individuals: 8828
  bin: 3.25e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 6.25e1
  variant carriers: 195
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 5.25e1
  variant carriers: 236
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 2.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 2.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 8136
  bin: 4.25e1
  variant carriers: 231
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.75e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 5.75e1
  variant carriers: 227
genotype quality: GenotypeQuality
num of homozygotes: 36
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

22-29669713-G-GTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669713
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669715
    reference: chr 22
allele count: 1
allele frequency: 8.620689655172414e-6
allele num: 116000
alternate allele: GTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.103-9_103-8dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.103-9_103-8dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.103-9_103-8dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.103-9_103-8dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.103-9_103-8dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.103-9_103-8dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1301_102+1302dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.167-9_167-8dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.103-6_103-5dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.103-6_103-5dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.530-9_530-8dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.103-9_103-8dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.127-9_127-8dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.103-6_103-5dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.97-9_97-8dupTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.103-9_103-8dupTT
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8136
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

22-29669713-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669713
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669713
    reference: chr 22
allele count: 2
allele frequency: 1.724137931034483e-5
allele num: 116000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.103-17G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.103-17G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.103-14G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.97-17G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.127-17G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.103-17G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.103-14G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.530-17G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.103-17G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.103-17G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.103-17G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.103-17G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.167-17G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1293G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.103-17G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.103-14G>T
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

22-29669713-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669713
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669712
    reference: chr 22
allele count: 65
allele frequency: 5.603448275862069e-4
allele num: 116000
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.103-8delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.103-8delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.103-8delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.103-8delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.103-5delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.103-5delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.103-8delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.127-8delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.530-8delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.97-8delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1302delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.103-5delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.103-8delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.103-8delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.167-8delT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.103-8delT
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8795
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8828
  bin: 3.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: GT
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD

22-29669718-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669718
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669718
    reference: chr 22
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.103-12T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.103-12T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.127-12T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.103-12T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.97-12T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.103-12T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.167-12T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.103-12T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.103-9T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.103-9T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.530-12T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1298T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.103-12T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.103-12T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.103-12T>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.103-9T>G
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

22-29669724-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669724
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669724
    reference: chr 22
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.127-6G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.103-6G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.167-6G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.103-6G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.103-6G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.103-6G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.103-6G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1304G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.530-6G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.103-3G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.103-6G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.103-6G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.103-3G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.103-6G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.103-3G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.97-6G>C
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6030
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10229
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.103-6G>C
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-29669725-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669725
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669725
    reference: chr 22
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.127-5A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.103-2A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.103-2A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.103-2A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.103-5A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.97-5A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.103-5A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.167-5A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.103-5A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.103-5A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.103-5A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.103-5A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.103-5A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.103-5A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.530-5A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1305A>G
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.103-2A>G
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

22-29669732-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669732
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669732
    reference: chr 22
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.105A>G
  hgvsp: ENST00000333395.6:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.105A>G
  hgvsp: ENST00000455726.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.105A>G
  hgvsp: ENST00000406548.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.105A>G
  hgvsp: ENST00000332050.6:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.129A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.105A>G
  hgvsp: ENST00000331029.7:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.105A>G
  hgvsp: ENST00000397938.2:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1312A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.99A>G
  hgvsp: ENST00000444626.1:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.108A>G
  hgvsp: ENST00000447973.1:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.105A>G
  hgvsp: ENST00000332035.6:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.169A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.105A>G
  hgvsp: ENST00000414183.2:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.532A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.108A>G
  hgvsp: ENST00000437155.2:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.108A>G
  hgvsp: ENST00000436425.1:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.105A>G
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/22-29669732-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669732
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669732
    reference: chr 22
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.105A>C
  hgvsp: ENST00000455726.1:c.105A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.108A>C
  hgvsp: ENST00000437155.2:c.108A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.169A>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.129A>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.108A>C
  hgvsp: ENST00000447973.1:c.108A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.105A>C
  hgvsp: ENST00000331029.7:c.105A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.105A>C
  hgvsp: ENST00000397938.2:c.105A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.108A>C
  hgvsp: ENST00000436425.1:c.108A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.105A>C
  hgvsp: ENST00000333395.6:c.105A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.105A>C
  hgvsp: ENST00000332050.6:c.105A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.105A>C
  hgvsp: ENST00000414183.2:c.105A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.105A>C
  hgvsp: ENST00000406548.1:c.105A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.99A>C
  hgvsp: ENST00000444626.1:c.99A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1312A>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.532A>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.105A>C
  hgvsp: ENST00000332035.6:c.105A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.105A>C
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

22-29669746-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669746
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669746
    reference: chr 22
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.122G>A
  hgvsp: ENSP00000405947.1:p.Ser41Asn
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.122G>A
  hgvsp: ENSP00000406824.1:p.Ser41Asn
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.119G>A
  hgvsp: ENSP00000400142.2:p.Ser40Asn
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.122G>A
  hgvsp: ENSP00000412670.2:p.Ser41Asn
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.119G>A
  hgvsp: ENSP00000393637.1:p.Ser40Asn
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.119G>A
  hgvsp: ENSP00000330896.6:p.Ser40Asn
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.119G>A
  hgvsp: ENSP00000385726.1:p.Ser40Asn
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.143G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1326G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.119G>A
  hgvsp: ENSP00000331699.6:p.Ser40Asn
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.183G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.546G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.119G>A
  hgvsp: ENSP00000381031.2:p.Ser40Asn
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.119G>A
  hgvsp: ENSP00000330516.7:p.Ser40Asn
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.119G>A
  hgvsp: ENSP00000327456.6:p.Ser40Asn
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.113G>A
  hgvsp: ENSP00000416171.1:p.Ser38Asn
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6030
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser40Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

22-29669749-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669749
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669749
    reference: chr 22
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.122A>G
  hgvsp: ENSP00000393637.1:p.Tyr41Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1329A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.122A>G
  hgvsp: ENSP00000330516.7:p.Tyr41Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.116A>G
  hgvsp: ENSP00000416171.1:p.Tyr39Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.122A>G
  hgvsp: ENSP00000400142.2:p.Tyr41Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.122A>G
  hgvsp: ENSP00000327456.6:p.Tyr41Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.122A>G
  hgvsp: ENSP00000381031.2:p.Tyr41Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.125A>G
  hgvsp: ENSP00000406824.1:p.Tyr42Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.125A>G
  hgvsp: ENSP00000405947.1:p.Tyr42Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.186A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.125A>G
  hgvsp: ENSP00000412670.2:p.Tyr42Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.122A>G
  hgvsp: ENSP00000385726.1:p.Tyr41Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.549A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.122A>G
  hgvsp: ENSP00000330896.6:p.Tyr41Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.146A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.122A>G
  hgvsp: ENSP00000331699.6:p.Tyr41Cys
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr41Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ

22-29669756-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669756
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669756
    reference: chr 22
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.123C>G
  hgvsp: ENST00000444626.1:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.129C>G
  hgvsp: ENST00000332050.6:c.129C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.129C>G
  hgvsp: ENST00000397938.2:c.129C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.129C>G
  hgvsp: ENST00000332035.6:c.129C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.129C>G
  hgvsp: ENST00000333395.6:c.129C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.132C>G
  hgvsp: ENST00000437155.2:c.132C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.556C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.132C>G
  hgvsp: ENST00000447973.1:c.132C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.129C>G
  hgvsp: ENST00000455726.1:c.129C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.129C>G
  hgvsp: ENST00000331029.7:c.129C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.132C>G
  hgvsp: ENST00000436425.1:c.132C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.193C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.129C>G
  hgvsp: ENST00000414183.2:c.129C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.129C>G
  hgvsp: ENST00000406548.1:c.129C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1336C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.153C>G
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr43Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

22-29669759-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669759
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669759
    reference: chr 22
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.559T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.135T>C
  hgvsp: ENST00000436425.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.156T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.132T>C
  hgvsp: ENST00000333395.6:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.135T>C
  hgvsp: ENST00000437155.2:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1339T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.132T>C
  hgvsp: ENST00000406548.1:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.135T>C
  hgvsp: ENST00000447973.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.132T>C
  hgvsp: ENST00000331029.7:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.126T>C
  hgvsp: ENST00000444626.1:c.126T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.132T>C
  hgvsp: ENST00000332035.6:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.132T>C
  hgvsp: ENST00000455726.1:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.132T>C
  hgvsp: ENST00000414183.2:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.132T>C
  hgvsp: ENST00000332050.6:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.132T>C
  hgvsp: ENST00000397938.2:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.196T>C
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr44Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

22-29669762-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669762
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669762
    reference: chr 22
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.138A>G
  hgvsp: ENST00000447973.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.135A>G
  hgvsp: ENST00000332035.6:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.135A>G
  hgvsp: ENST00000333395.6:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.199A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.135A>G
  hgvsp: ENST00000331029.7:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.135A>G
  hgvsp: ENST00000455726.1:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.138A>G
  hgvsp: ENST00000437155.2:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.135A>G
  hgvsp: ENST00000414183.2:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000493426
  gene symbol: EWSR1
  hgvsc: ENST00000493426.1:n.562A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.159A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.135A>G
  hgvsp: ENST00000397938.2:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.135A>G
  hgvsp: ENST00000332050.6:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.138A>G
  hgvsp: ENST00000436425.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.129A>G
  hgvsp: ENST00000444626.1:c.129A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1342A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.135A>G
  hgvsp: ENST00000406548.1:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly45Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

22-29669785-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669785
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669785
    reference: chr 22
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.158C>G
  hgvsp: ENSP00000327456.6:p.Thr53Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.182C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.161C>G
  hgvsp: ENSP00000405947.1:p.Thr54Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.161C>G
  hgvsp: ENSP00000406824.1:p.Thr54Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.152C>G
  hgvsp: ENSP00000416171.1:p.Thr51Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.161C>G
  hgvsp: ENSP00000412670.2:p.Thr54Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.158C>G
  hgvsp: ENSP00000330516.7:p.Thr53Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.158C>G
  hgvsp: ENSP00000381031.2:p.Thr53Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.222C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.158C>G
  hgvsp: ENSP00000400142.2:p.Thr53Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.158C>G
  hgvsp: ENSP00000385726.1:p.Thr53Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.158C>G
  hgvsp: ENSP00000393637.1:p.Thr53Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1365C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.158C>G
  hgvsp: ENSP00000330896.6:p.Thr53Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.158C>G
  hgvsp: ENSP00000331699.6:p.Thr53Ser
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10976
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr53Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

22-29669793-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669793
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669793
    reference: chr 22
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.166C>G
  hgvsp: ENSP00000331699.6:p.Gln56Glu
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.230C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.160C>G
  hgvsp: ENSP00000416171.1:p.Gln54Glu
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.166C>G
  hgvsp: ENSP00000330896.6:p.Gln56Glu
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.166C>G
  hgvsp: ENSP00000381031.2:p.Gln56Glu
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1373C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.169C>G
  hgvsp: ENSP00000406824.1:p.Gln57Glu
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.166C>G
  hgvsp: ENSP00000327456.6:p.Gln56Glu
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.169C>G
  hgvsp: ENSP00000412670.2:p.Gln57Glu
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.166C>G
  hgvsp: ENSP00000393637.1:p.Gln56Glu
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.166C>G
  hgvsp: ENSP00000330516.7:p.Gln56Glu
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.166C>G
  hgvsp: ENSP00000385726.1:p.Gln56Glu
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.166C>G
  hgvsp: ENSP00000400142.2:p.Gln56Glu
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.169C>G
  hgvsp: ENSP00000405947.1:p.Gln57Glu
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.190C>G
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6030
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln56Glu
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

22-29669795-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669795
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669795
    reference: chr 22
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.171G>C
  hgvsp: ENSP00000412670.2:p.Gln57His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.162G>C
  hgvsp: ENSP00000416171.1:p.Gln54His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.192G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.168G>C
  hgvsp: ENSP00000327456.6:p.Gln56His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.171G>C
  hgvsp: ENSP00000405947.1:p.Gln57His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.168G>C
  hgvsp: ENSP00000381031.2:p.Gln56His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.168G>C
  hgvsp: ENSP00000400142.2:p.Gln56His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.168G>C
  hgvsp: ENSP00000331699.6:p.Gln56His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.232G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.171G>C
  hgvsp: ENSP00000406824.1:p.Gln57His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.168G>C
  hgvsp: ENSP00000330516.7:p.Gln56His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1375G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.168G>C
  hgvsp: ENSP00000385726.1:p.Gln56His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.168G>C
  hgvsp: ENSP00000330896.6:p.Gln56His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.168G>C
  hgvsp: ENSP00000393637.1:p.Gln56His
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln56His
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-29669799-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669799
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669799
    reference: chr 22
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.172A>C
  hgvsp: ENSP00000330896.6:p.Thr58Pro
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.175A>C
  hgvsp: ENSP00000405947.1:p.Thr59Pro
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1379A>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.236A>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.172A>C
  hgvsp: ENSP00000381031.2:p.Thr58Pro
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.172A>C
  hgvsp: ENSP00000385726.1:p.Thr58Pro
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.172A>C
  hgvsp: ENSP00000400142.2:p.Thr58Pro
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.172A>C
  hgvsp: ENSP00000393637.1:p.Thr58Pro
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.172A>C
  hgvsp: ENSP00000330516.7:p.Thr58Pro
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.175A>C
  hgvsp: ENSP00000412670.2:p.Thr59Pro
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.175A>C
  hgvsp: ENSP00000406824.1:p.Thr59Pro
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.172A>C
  hgvsp: ENSP00000331699.6:p.Thr58Pro
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.172A>C
  hgvsp: ENSP00000327456.6:p.Thr58Pro
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.166A>C
  hgvsp: ENSP00000416171.1:p.Thr56Pro
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.196A>C
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10281
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr58Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-29669807-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669807
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669807
    reference: chr 22
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.183C>T
  hgvsp: ENST00000436425.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.183C>T
  hgvsp: ENST00000437155.2:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.180C>T
  hgvsp: ENST00000406548.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1387C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.180C>T
  hgvsp: ENST00000397938.2:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.244C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.180C>T
  hgvsp: ENST00000332035.6:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.174C>T
  hgvsp: ENST00000444626.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.180C>T
  hgvsp: ENST00000332050.6:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.180C>T
  hgvsp: ENST00000414183.2:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.204C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.180C>T
  hgvsp: ENST00000333395.6:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.183C>T
  hgvsp: ENST00000447973.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.180C>T
  hgvsp: ENST00000455726.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.180C>T
  hgvsp: ENST00000331029.7:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr60Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-29669816-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669816
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669816
    reference: chr 22
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.183G>C
  hgvsp: ENSP00000416171.1:p.Gln61His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.189G>C
  hgvsp: ENSP00000400142.2:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.189G>C
  hgvsp: ENSP00000330516.7:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.189G>C
  hgvsp: ENSP00000393637.1:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.253G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.189G>C
  hgvsp: ENSP00000331699.6:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.192G>C
  hgvsp: ENSP00000412670.2:p.Gln64His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.192G>C
  hgvsp: ENSP00000405947.1:p.Gln64His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.213G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.189G>C
  hgvsp: ENSP00000327456.6:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.189G>C
  hgvsp: ENSP00000381031.2:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.189G>C
  hgvsp: ENSP00000330896.6:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.192G>C
  hgvsp: ENSP00000406824.1:p.Gln64His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.189G>C
  hgvsp: ENSP00000385726.1:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1396G>C
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln63His
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

22-29669816-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669816
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669816
    reference: chr 22
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.189G>T
  hgvsp: ENSP00000393637.1:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.189G>T
  hgvsp: ENSP00000385726.1:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.189G>T
  hgvsp: ENSP00000381031.2:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.189G>T
  hgvsp: ENSP00000330516.7:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.189G>T
  hgvsp: ENSP00000330896.6:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.192G>T
  hgvsp: ENSP00000412670.2:p.Gln64His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1396G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.189G>T
  hgvsp: ENSP00000327456.6:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.189G>T
  hgvsp: ENSP00000400142.2:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.189G>T
  hgvsp: ENSP00000331699.6:p.Gln63His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.192G>T
  hgvsp: ENSP00000406824.1:p.Gln64His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.183G>T
  hgvsp: ENSP00000416171.1:p.Gln61His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.192G>T
  hgvsp: ENSP00000405947.1:p.Gln64His
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.213G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.253G>T
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6030
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln63His
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

22-29669817-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669817
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669817
    reference: chr 22
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.190A>T
  hgvsp: ENSP00000331699.6:p.Thr64Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.190A>T
  hgvsp: ENSP00000385726.1:p.Thr64Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1397A>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.190A>T
  hgvsp: ENSP00000330896.6:p.Thr64Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.193A>T
  hgvsp: ENSP00000412670.2:p.Thr65Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.190A>T
  hgvsp: ENSP00000381031.2:p.Thr64Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.254A>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.193A>T
  hgvsp: ENSP00000405947.1:p.Thr65Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.184A>T
  hgvsp: ENSP00000416171.1:p.Thr62Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.190A>T
  hgvsp: ENSP00000327456.6:p.Thr64Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.190A>T
  hgvsp: ENSP00000400142.2:p.Thr64Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.214A>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.193A>T
  hgvsp: ENSP00000406824.1:p.Thr65Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.190A>T
  hgvsp: ENSP00000393637.1:p.Thr64Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.190A>T
  hgvsp: ENSP00000330516.7:p.Thr64Ser
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr64Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

22-29669819-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669819
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669819
    reference: chr 22
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.192C>T
  hgvsp: ENST00000332035.6:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.192C>T
  hgvsp: ENST00000406548.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.192C>T
  hgvsp: ENST00000414183.2:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.192C>T
  hgvsp: ENST00000333395.6:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1399C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.186C>T
  hgvsp: ENST00000444626.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.192C>T
  hgvsp: ENST00000332050.6:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.195C>T
  hgvsp: ENST00000447973.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.195C>T
  hgvsp: ENST00000437155.2:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.192C>T
  hgvsp: ENST00000397938.2:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.192C>T
  hgvsp: ENST00000331029.7:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.192C>T
  hgvsp: ENST00000455726.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.216C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.195C>T
  hgvsp: ENST00000436425.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.256C>T
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10285
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr64Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-29669824-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669824
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669824
    reference: chr 22
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.197A>G
  hgvsp: ENSP00000381031.2:p.Tyr66Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.200A>G
  hgvsp: ENSP00000406824.1:p.Tyr67Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.197A>G
  hgvsp: ENSP00000331699.6:p.Tyr66Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.200A>G
  hgvsp: ENSP00000405947.1:p.Tyr67Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.200A>G
  hgvsp: ENSP00000412670.2:p.Tyr67Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.197A>G
  hgvsp: ENSP00000327456.6:p.Tyr66Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.221A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.197A>G
  hgvsp: ENSP00000385726.1:p.Tyr66Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.197A>G
  hgvsp: ENSP00000393637.1:p.Tyr66Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.197A>G
  hgvsp: ENSP00000400142.2:p.Tyr66Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.197A>G
  hgvsp: ENSP00000330896.6:p.Tyr66Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1404A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.197A>G
  hgvsp: ENSP00000330516.7:p.Tyr66Cys
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.261A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.191A>G
  hgvsp: ENSP00000416171.1:p.Tyr64Cys
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9737
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr66Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

22-29669828-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669828
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669828
    reference: chr 22
allele count: 7
allele frequency: 5.767772980455489e-5
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.201A>G
  hgvsp: ENST00000333395.6:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.201A>G
  hgvsp: ENST00000397938.2:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.201A>G
  hgvsp: ENST00000406548.1:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.201A>G
  hgvsp: ENST00000332050.6:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.265A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1408A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.204A>G
  hgvsp: ENST00000447973.1:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.195A>G
  hgvsp: ENST00000444626.1:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.201A>G
  hgvsp: ENST00000414183.2:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.201A>G
  hgvsp: ENST00000331029.7:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.225A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.204A>G
  hgvsp: ENST00000437155.2:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.201A>G
  hgvsp: ENST00000455726.1:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.204A>G
  hgvsp: ENST00000436425.1:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.201A>G
  hgvsp: ENST00000332035.6:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9738
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala67Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS

22-29669829-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669829
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669829
    reference: chr 22
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1409A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.202A>G
  hgvsp: ENSP00000381031.2:p.Thr68Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.205A>G
  hgvsp: ENSP00000406824.1:p.Thr69Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.205A>G
  hgvsp: ENSP00000405947.1:p.Thr69Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.202A>G
  hgvsp: ENSP00000330516.7:p.Thr68Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.202A>G
  hgvsp: ENSP00000331699.6:p.Thr68Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.226A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.202A>G
  hgvsp: ENSP00000385726.1:p.Thr68Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.205A>G
  hgvsp: ENSP00000412670.2:p.Thr69Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.266A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.202A>G
  hgvsp: ENSP00000330896.6:p.Thr68Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.202A>G
  hgvsp: ENSP00000400142.2:p.Thr68Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.202A>G
  hgvsp: ENSP00000327456.6:p.Thr68Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.202A>G
  hgvsp: ENSP00000393637.1:p.Thr68Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.196A>G
  hgvsp: ENSP00000416171.1:p.Thr66Ala
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6027
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr68Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

22-29669837-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669837
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669837
    reference: chr 22
allele count: 2
allele frequency: 1.648043772042586e-5
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.210T>C
  hgvsp: ENST00000332035.6:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1417T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.204T>C
  hgvsp: ENST00000444626.1:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.210T>C
  hgvsp: ENST00000397938.2:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.213T>C
  hgvsp: ENST00000447973.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.213T>C
  hgvsp: ENST00000437155.2:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.210T>C
  hgvsp: ENST00000332050.6:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.210T>C
  hgvsp: ENST00000455726.1:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.213T>C
  hgvsp: ENST00000436425.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.210T>C
  hgvsp: ENST00000406548.1:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.210T>C
  hgvsp: ENST00000333395.6:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.210T>C
  hgvsp: ENST00000331029.7:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.274T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.210T>C
  hgvsp: ENST00000414183.2:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.234T>C
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6024
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr70Tyr
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

22-29669840-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669840
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669840
    reference: chr 22
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.213A>G
  hgvsp: ENST00000414183.2:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.216A>G
  hgvsp: ENST00000437155.2:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.213A>G
  hgvsp: ENST00000332035.6:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.216A>G
  hgvsp: ENST00000447973.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.213A>G
  hgvsp: ENST00000333395.6:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.213A>G
  hgvsp: ENST00000397938.2:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.213A>G
  hgvsp: ENST00000455726.1:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.213A>G
  hgvsp: ENST00000406548.1:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.216A>G
  hgvsp: ENST00000436425.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.213A>G
  hgvsp: ENST00000331029.7:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.207A>G
  hgvsp: ENST00000444626.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.277A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1420A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.213A>G
  hgvsp: ENST00000332050.6:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.237A>G
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9732
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly71Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

22-29669847-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669847
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669847
    reference: chr 22
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.220C>T
  hgvsp: ENSP00000330896.6:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.284C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.214C>T
  hgvsp: ENSP00000416171.1:p.Pro72Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.223C>T
  hgvsp: ENSP00000406824.1:p.Pro75Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.223C>T
  hgvsp: ENSP00000405947.1:p.Pro75Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.220C>T
  hgvsp: ENSP00000327456.6:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.220C>T
  hgvsp: ENSP00000385726.1:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.220C>T
  hgvsp: ENSP00000331699.6:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.220C>T
  hgvsp: ENSP00000381031.2:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.244C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.220C>T
  hgvsp: ENSP00000330516.7:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.223C>T
  hgvsp: ENSP00000412670.2:p.Pro75Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.220C>T
  hgvsp: ENSP00000393637.1:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1427C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.220C>T
  hgvsp: ENSP00000400142.2:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro74Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

22-29669850-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669850
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669850
    reference: chr 22
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.226A>G
  hgvsp: ENSP00000405947.1:p.Thr76Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.223A>G
  hgvsp: ENSP00000327456.6:p.Thr75Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.223A>G
  hgvsp: ENSP00000400142.2:p.Thr75Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.287A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.223A>G
  hgvsp: ENSP00000330516.7:p.Thr75Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.223A>G
  hgvsp: ENSP00000381031.2:p.Thr75Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.223A>G
  hgvsp: ENSP00000385726.1:p.Thr75Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.226A>G
  hgvsp: ENSP00000406824.1:p.Thr76Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.247A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.223A>G
  hgvsp: ENSP00000393637.1:p.Thr75Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.226A>G
  hgvsp: ENSP00000412670.2:p.Thr76Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.223A>G
  hgvsp: ENSP00000331699.6:p.Thr75Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.217A>G
  hgvsp: ENSP00000416171.1:p.Thr73Ala
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1430A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.223A>G
  hgvsp: ENSP00000330896.6:p.Thr75Ala
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10901
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr75Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

22-29669860-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669860
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669860
    reference: chr 22
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.290+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1440C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.229+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.226+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.229+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+7C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+7C>T
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10188
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.226+7C>T
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-29669865-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669865
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669865
    reference: chr 22
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.290+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1445C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.229+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.229+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+12C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.226+12C>T
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10152
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-29669883-TCGTTCTGG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669883
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669875
    reference: chr 22
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10396
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6007
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: TCGTTCTGG
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

22-29669884-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669884
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669884
    reference: chr 22
allele count: 2
allele frequency: 1.650818806127839e-5
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.229+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1464C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.290+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.229+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.226+31C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+31C>T
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6005
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum

22-29669885-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669885
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669885
    reference: chr 22
allele count: 23
allele frequency: 1.898504308779344e-4
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.229+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1465G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.226+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.290+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+32G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.229+32G>A
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9603
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6005
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

22-29669892-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669892
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669892
    reference: chr 22
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1472C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.229+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.229+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.226+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.290+39C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+39C>G
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

22-29669893-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669893
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669893
    reference: chr 22
allele count: 1
allele frequency: 8.257774694875225e-6
allele num: 121098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.290+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.229+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1473T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.229+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+40T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.226+40T>A
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8449
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

22-29669894-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669894
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669894
    reference: chr 22
allele count: 1
allele frequency: 8.256683785524381e-6
allele num: 121114
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.226+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.229+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.290+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.229+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1474A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+41A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+41A>G
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9561
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-29669897-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669897
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669897
    reference: chr 22
allele count: 2
allele frequency: 1.652400938563733e-5
allele num: 121036
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.290+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.229+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1477G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.226+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.229+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+44G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+44G>A
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8239
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9543
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-29669898-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669898
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669899
    reference: chr 22
allele count: 109
allele frequency: 9.010498470695214e-4
allele num: 120970
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.290+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.229+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1479dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.229+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+46dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.226+46dupA
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7792
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 9533
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 4.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-29669901-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29669901
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29669901
    reference: chr 22
allele count: 343
allele frequency: 2.834148598625066e-3
allele num: 121024
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.226+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.290+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.229+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1481T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+48T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.229+48T>C
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 5.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9470
  bin: 3.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7490
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 6.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD

22-29670212-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670212
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670212
    reference: chr 22
allele count: 1
allele frequency: 8.314210648840998e-6
allele num: 120276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+359C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+359C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+359C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+359C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+359C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.230-42C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+359C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.291-42C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+359C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1792C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+359C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+359C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.230-45C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.227-42C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+359C>G
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

22-29670226-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670226
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670226
    reference: chr 22
allele count: 1
allele frequency: 8.314072398942449e-6
allele num: 120278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+373T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.291-28T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.227-28T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+373T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+373T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+373T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+373T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+373T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.230-31T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.230-28T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1806T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+373T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+373T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+373T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+373T>C
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

22-29670232-TTTTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670232
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670228
    reference: chr 22
allele count: 1
allele frequency: 8.313934153641504e-6
allele num: 120280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+383_226+386delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+383_226+386delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.291-18_291-15delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.230-18_230-15delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1816_102+1819delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.230-21_230-18delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+383_226+386delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+383_226+386delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+383_229+386delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+383_226+386delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+383_250+386delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+383_226+386delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.227-18_227-15delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+383_220+386delGTTT
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+383_226+386delGTTT
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: TTTTG
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

22-29670233-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670233
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670233
    reference: chr 22
allele count: 1
allele frequency: 8.314072398942449e-6
allele num: 120278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+380T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+380T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.291-21T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+380T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+380T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1813T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+380T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+380T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+380T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+380T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.227-21T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.230-21T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+380T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+380T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.230-24T>C
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

22-29670237-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670237
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670237
    reference: chr 22
allele count: 1
allele frequency: 8.313934153641504e-6
allele num: 120280
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.227-17T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+384T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1817T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+384T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+384T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.291-17T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+384T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+384T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+384T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+384T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+384T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.230-20T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+384T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+384T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.230-17T>A
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

22-29670244-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670244
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670244
    reference: chr 22
allele count: 1
allele frequency: 8.313795912937929e-6
allele num: 120282
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.227-10C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.291-10C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+391C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+391C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+391C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.230-10C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+391C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+391C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+391C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1824C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+391C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.230-13C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+391C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+391C>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+391C>T
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

22-29670259-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670259
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670259
    reference: chr 22
allele count: 2
allele frequency: 1.662759182587586e-5
allele num: 120282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+406G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.235G>A
  hgvsp: ENSP00000406824.1:p.Gly79Arg
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+406G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1839G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+406G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.296G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+406G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+406G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.232G>A
  hgvsp: ENSP00000405947.1:p.Gly78Arg
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.232G>A
  hgvsp: ENSP00000400142.2:p.Gly78Arg
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+406G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+406G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+406G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+406G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+406G>A
  variant of: http://identifiers.org/hgnc/3508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20634
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4518
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly78Arg
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

22-29670280-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670280
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670280
    reference: chr 22
allele count: 5
allele frequency: 4.15682883841575e-5
allele num: 120284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+427A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+427A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+427A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+427A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.247+9A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.317A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+427A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.244+9A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+427A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+427A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+427A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1860A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+427A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.244+9A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+427A>G
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4518
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20636
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

22-29670284-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670284
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670284
    reference: chr 22
allele count: 1
allele frequency: 8.313657676831499e-6
allele num: 120284
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.244+13T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+431T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+431T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+431T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.321T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+431T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1864T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+431T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+431T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+431T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.244+13T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.247+13T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+431T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+431T>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+431T>C
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

22-29670289-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670289
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670289
    reference: chr 22
allele count: 1
allele frequency: 8.313657676831499e-6
allele num: 120284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+436A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.247+18A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+436A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.326A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1869A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+436A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+436A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.244+18A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.244+18A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+436A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+436A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+436A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+436A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+436A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+436A>G
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

22-29670295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670295
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670295
    reference: chr 22
allele count: 1
allele frequency: 8.313657676831499e-6
allele num: 120284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+442G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+442G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+442G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+442G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+442G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.244+24G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+442G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+442G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+442G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.332G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+442G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.247+24G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+442G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1875G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.244+24G>A
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20634
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-29670296-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670296
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670296
    reference: chr 22
allele count: 1
allele frequency: 8.313657676831499e-6
allele num: 120284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.244+25C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+443C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+443C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+443C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+443C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+443C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+443C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.333C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.247+25C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1876C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+443C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+443C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.244+25C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+443C>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+443C>A
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20634
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

22-29670313-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670313
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670313
    reference: chr 22
allele count: 1
allele frequency: 8.313934153641504e-6
allele num: 120280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+460A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+460A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.350A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+460A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+460A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+460A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+460A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1893A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+460A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.244+42A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.244+42A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.247+42A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+460A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+460A>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+460A>G
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-29670314-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670314
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670314
    reference: chr 22
allele count: 1
allele frequency: 8.313934153641504e-6
allele num: 120280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+461T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1894T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+461T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.244+43T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+461T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.247+43T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.351T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+461T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+461T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.244+43T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+461T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+461T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+461T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+461T>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+461T>A
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

22-29670320-C-CTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670320
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670322
    reference: chr 22
allele count: 15
allele frequency: 1.247110859841368e-4
allele num: 120278
alternate allele: CTA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.247+50_247+51dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.358_359dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+468_226+469dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.244+50_244+51dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+468_226+469dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+468_250+469dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+468_229+469dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1901_102+1902dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+468_226+469dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+468_220+469dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+468_226+469dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+468_226+469dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+468_226+469dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+468_226+469dupTA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.244+50_244+51dupTA
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20634
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

22-29670320-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670320
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670320
    reference: chr 22
allele count: 2
allele frequency: 1.66281447978849e-5
allele num: 120278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+467C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+467C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+467C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.244+49C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.244+49C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+467C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+467C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+467C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1900C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.357C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+467C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+467C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+467C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+467C>G
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.247+49C>G
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS

22-29670321-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29670321
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29670322
    reference: chr 22
allele count: 1
allele frequency: 8.316146630297385e-6
allele num: 120248
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.226+470dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.226+470dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.102+1903dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.244+52dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.226+470dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.226+470dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.247+52dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000485037
  gene symbol: EWSR1
  hgvsc: ENST00000485037.1:n.360dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.220+470dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.226+470dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.244+52dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.226+470dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.226+470dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.229+470dupA
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.250+470dupA
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

22-29673968-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29673968
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29673968
    reference: chr 22
allele count: 3
allele frequency: 2.673987450085568e-5
allele num: 112192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.221-51G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.227-51G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.227-51G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.103-152G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.245-51G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000479135
  gene symbol: EWSR1
  hgvsc: ENST00000479135.1:n.2351G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.251-51G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.227-51G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.245-51G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.248-51G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.227-51G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.227-51G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.227-51G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.230-51G>C
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.227-51G>C
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3958
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17417
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

22-29673972-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29673972
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29673972
    reference: chr 22
allele count: 3
allele frequency: 2.666666666666667e-5
allele num: 112500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.248-47G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.221-47G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.227-47G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.227-47G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.227-47G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000479135
  gene symbol: EWSR1
  hgvsc: ENST00000479135.1:n.2355G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.245-47G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.227-47G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.103-148G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.251-47G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.227-47G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.227-47G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.230-47G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.227-47G>T
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.245-47G>T
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12702
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

22-29673983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29673983
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 29673983
    reference: chr 22
allele count: 1
allele frequency: 8.830022075055188e-6
allele num: 113250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000479135
  gene symbol: EWSR1
  hgvsc: ENST00000479135.1:n.2366G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000405947
  ensembl transcript: ENST00000447973
  gene symbol: EWSR1
  hgvsc: ENST00000447973.1:c.245-36G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000406824
  ensembl transcript: ENST00000436425
  gene symbol: EWSR1
  hgvsc: ENST00000436425.1:c.248-36G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000385726
  ensembl transcript: ENST00000406548
  gene symbol: EWSR1
  hgvsc: ENST00000406548.1:c.227-36G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000416171
  ensembl transcript: ENST00000444626
  gene symbol: EWSR1
  hgvsc: ENST00000444626.1:c.221-36G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl transcript: ENST00000483415
  gene symbol: EWSR1
  hgvsc: ENST00000483415.1:n.251-36G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000331699
  ensembl transcript: ENST00000332035
  gene symbol: EWSR1
  hgvsc: ENST00000332035.6:c.227-36G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330516
  ensembl transcript: ENST00000331029
  gene symbol: EWSR1
  hgvsc: ENST00000331029.7:c.227-36G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000327456
  ensembl transcript: ENST00000333395
  gene symbol: EWSR1
  hgvsc: ENST00000333395.6:c.227-36G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000381031
  ensembl transcript: ENST00000397938
  gene symbol: EWSR1
  hgvsc: ENST00000397938.2:c.227-36G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000400142
  ensembl transcript: ENST00000414183
  gene symbol: EWSR1
  hgvsc: ENST00000414183.2:c.245-36G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000393637
  ensembl transcript: ENST00000455726
  gene symbol: EWSR1
  hgvsc: ENST00000455726.1:c.227-36G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000330896
  ensembl transcript: ENST00000332050
  gene symbol: EWSR1
  hgvsc: ENST00000332050.6:c.227-36G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000395200
  ensembl transcript: ENST00000415761
  gene symbol: EWSR1
  hgvsc: ENST00000415761.1:c.103-137G>A
  variant of: http://identifiers.org/hgnc/3508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182944
  ensembl protein: ENSP00000412670
  ensembl transcript: ENST00000437155
  gene symbol: EWSR1
  hgvsc: ENST00000437155.2:c.230-36G>A
  variant of: http://identifiers.org/hgnc/3508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: QD

GenotypeDepth
all individuals: 9253
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 299
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2593
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4712
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 363
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7844
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1149
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 523
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1636
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4674
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5261
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4473
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3916
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9456
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2654
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26108
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.911e0

FS
type: SiteQuality
SIO_000300: 3.061e0

MQ
type: SiteQuality
SIO_000300: 5.735e1

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

DP
type: SiteQuality
SIO_000300: 2.555368e6

QD
type: SiteQuality
SIO_000300: 7.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

GenotypeDepth
all individuals: 6138
bin: 4.75e1
variant carriers: 741

GenotypeDepth
all individuals: 1124
bin: 7.25e1
variant carriers: 366

GenotypeDepth
all individuals: 1514
bin: 6.75e1
variant carriers: 490

GenotypeDepth
all individuals: 8247
bin: 2.75e1
variant carriers: 207

GenotypeDepth
all individuals: 782
bin: 7.75e1
variant carriers: 247

GenotypeDepth
all individuals: 113
bin: 1.25e1
variant carriers: 7

GenotypeDepth
all individuals: 338
bin: 9.25e1
variant carriers: 103

GenotypeDepth
all individuals: 418
bin: 8.75e1
variant carriers: 118

GenotypeDepth
all individuals: 602
bin: 8.25e1
variant carriers: 166

GenotypeDepth
all individuals: 4410
bin: 5.25e1
variant carriers: 782

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3016
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2431
bin: 8.75e1
variant carriers: 7

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 4249
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 3528
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 4855
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8739
bin: 6.25e1
variant carriers: 6

GenotypeQuality
all individuals: 4061
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 108
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 29016
bin: 9.75e1
variant carriers: 6960

European (Finnish)
type: Population
allele count: 491
allele frequency: 7.44164898454077e-2
allele num: 6598
num of homozygotes: 12

African
type: Population
allele count: 140
allele frequency: 1.347190146266359e-2
allele num: 10392
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 6055
allele frequency: 9.088316522574448e-2
allele num: 66624
num of homozygotes: 277

Other
type: Population
allele count: 51
allele frequency: 5.616740088105727e-2
allele num: 908
num of homozygotes: 1

South Asian
type: Population
allele count: 224
allele frequency: 1.360048573163327e-2
allele num: 16470
num of homozygotes: 7

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

Latino
type: Population
allele count: 356
allele frequency: 3.079052067116416e-2
allele num: 11562
num of homozygotes: 9

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.78e-2

DP
type: SiteQuality
SIO_000300: 2.694928e6

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

FS
type: SiteQuality
SIO_000300: 6.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.814e1

QD
type: SiteQuality
SIO_000300: 1.454e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.25e-1

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeDepth
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bin: 4.75e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 908
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variant carriers: 0

GenotypeQuality
all individuals: 3273
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.201056930098487e-4
allele num: 8326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14894
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558895055184885e-5
allele num: 64148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.17e0

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

DP
type: SiteQuality
SIO_000300: 2.744632e6

MQ
type: SiteQuality
SIO_000300: 5.827e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.46e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

GenotypeDepth
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bin: 4.75e1
variant carriers: 249

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 209

GenotypeDepth
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GenotypeDepth
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variant carriers: 74

GenotypeDepth
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variant carriers: 33

GenotypeDepth
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GenotypeDepth
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variant carriers: 107

GenotypeDepth
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 7

GenotypeQuality
all individuals: 462
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variant carriers: 36

GenotypeQuality
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variant carriers: 11

GenotypeQuality
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GenotypeQuality
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variant carriers: 28

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 13

GenotypeQuality
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variant carriers: 42

GenotypeQuality
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bin: 2.75e1
variant carriers: 21

GenotypeQuality
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variant carriers: 48

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 18

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 1979

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 4687
bin: 6.75e1
variant carriers: 2

East Asian
type: Population
allele count: 12
allele frequency: 1.441268316118184e-3
allele num: 8326
num of homozygotes: 0

Latino
type: Population
allele count: 55
allele frequency: 4.899340815962943e-3
allele num: 11226
num of homozygotes: 0

African
type: Population
allele count: 30
allele frequency: 2.992817238627295e-3
allele num: 10024
num of homozygotes: 0

Other
type: Population
allele count: 16
allele frequency: 1.84331797235023e-2
allele num: 868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 390
allele frequency: 5.987104697574455e-2
allele num: 6514
num of homozygotes: 11

South Asian
type: Population
allele count: 163
allele frequency: 1.094400429703236e-2
allele num: 14894
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 1475
allele frequency: 2.299370206397705e-2
allele num: 64148
num of homozygotes: 23

BaseQRankSum
type: SiteQuality
SIO_000300: -4.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.17e0

QD
type: SiteQuality
SIO_000300: 8.67e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

DP
type: SiteQuality
SIO_000300: 2.744632e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.46e-2

MQ
type: SiteQuality
SIO_000300: 5.827e1

GenotypeDepth
all individuals: 8828
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558895055184885e-5
allele num: 64148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.17e0

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.6e-1

QD
type: SiteQuality
SIO_000300: 8.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.46e-2

DP
type: SiteQuality
SIO_000300: 2.744632e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.827e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
all individuals: 2455
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.402113860196973e-4
allele num: 8326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64148
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

ClippingRankSum
type: SiteQuality
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QD
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VQSLOD
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FS
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MQ
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.46e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.6e-1

DP
type: SiteQuality
SIO_000300: 2.744632e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 28

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeQuality
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variant carriers: 11

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 19

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 2

East Asian
type: Population
allele count: 4
allele frequency: 4.804227720393946e-4
allele num: 8326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 43
allele frequency: 6.703248737295006e-4
allele num: 64148
num of homozygotes: 0

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

South Asian
type: Population
allele count: 8
allele frequency: 5.37129045253122e-4
allele num: 14894
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.781578478531979e-4
allele num: 11226
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.983240223463687e-4
allele num: 10024
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.152073732718894e-3
allele num: 868
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.17e0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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DP
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MQ
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FS
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.6e-1

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4860
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GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
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European (Non-Finnish)
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FS
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InbreedingCoeff
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MQ
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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DP
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VQSLOD
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QD
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FS
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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East Asian
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FS
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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VQSLOD
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DP
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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ClippingRankSum
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FS
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ReadPosRankSum
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VQSLOD
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QD
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DP
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VQSLOD
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East Asian
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African
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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African
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South Asian
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European (Finnish)
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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FS
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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Other
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South Asian
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Latino
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European (Finnish)
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BaseQRankSum
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DP
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 11570
num of homozygotes: 0

South Asian
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African
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East Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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MQRankSum
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FS
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QD
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ReadPosRankSum
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VQSLOD
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DP
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InbreedingCoeff
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MQ
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

East Asian
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African
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Latino
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European (Non-Finnish)
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Other
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South Asian
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MQ
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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FS
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QD
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GenotypeDepth
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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South Asian
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VQSLOD
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DP
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ClippingRankSum
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InbreedingCoeff
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FS
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QD
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MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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East Asian
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Other
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QD
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BaseQRankSum
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FS
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MQRankSum
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InbreedingCoeff
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MQ
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DP
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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East Asian
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DP
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FS
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MQ
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VQSLOD
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MQRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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FS
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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African
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East Asian
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European (Non-Finnish)
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South Asian
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QD
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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DP
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BaseQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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Latino
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East Asian
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MQRankSum
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SIO_000300: -8.699999999999999e-2

FS
type: SiteQuality
SIO_000300: 3.821e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.826e1

MQ
type: SiteQuality
SIO_000300: 5.645e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.027e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 2.491907e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.928e0

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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SIO_000300: 5.988e1

DP
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SIO_000300: 2.491778e6

VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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ClippingRankSum
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SIO_000300: 1.9e0

ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 3.54e0

DP
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SIO_000300: 2.49157e6

ClippingRankSum
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SIO_000300: -8.94e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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SIO_000300: 1.79e0

MQ
type: SiteQuality
SIO_000300: 5.889e1

BaseQRankSum
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SIO_000300: 3.08e0

VQSLOD
type: SiteQuality
SIO_000300: -8.675e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.8e-1

QD
type: SiteQuality
SIO_000300: 1.188e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 8.993075331994364e-5
allele num: 66718
num of homozygotes: 0

African
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allele count: 1
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allele num: 10406
num of homozygotes: 0

Other
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num of homozygotes: 0

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

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

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

InbreedingCoeff
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SIO_000300: -2.0e-4

DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.899e1

FS
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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

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

Other
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African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

QD
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DP
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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MQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 908
num of homozygotes: 0

Latino
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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South Asian
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ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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DP
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VQSLOD
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QD
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
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allele num: 11560
num of homozygotes: 0

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

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

Other
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South Asian
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African
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East Asian
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European (Non-Finnish)
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Latino
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BaseQRankSum
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SIO_000300: 7.53e-1

ReadPosRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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InbreedingCoeff
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FS
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VQSLOD
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MQRankSum
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QD
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ClippingRankSum
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DP
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MQ
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Other
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African
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Latino
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South Asian
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InbreedingCoeff
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QD
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FS
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ClippingRankSum
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VQSLOD
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DP
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MQRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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South Asian
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African
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ReadPosRankSum
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QD
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FS
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BaseQRankSum
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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Latino
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European (Non-Finnish)
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African
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South Asian
type: Population
allele count: 1
allele frequency: 6.090133982947625e-5
allele num: 16420
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 1.1e1

MQRankSum
type: SiteQuality
SIO_000300: 3.76e-1

DP
type: SiteQuality
SIO_000300: 2.463899e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 8252
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variant carriers: 2

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 23

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3577
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variant carriers: 0

GenotypeQuality
all individuals: 5701
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.089392278650591e-5
allele num: 16422
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 2.852338917912688e-4
allele num: 66612
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.873e1

MQRankSum
type: SiteQuality
SIO_000300: 4.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.359e0

FS
type: SiteQuality
SIO_000300: 2.183e0

QD
type: SiteQuality
SIO_000300: 1.361e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.44e-1

DP
type: SiteQuality
SIO_000300: 2.460437e6

GenotypeDepth
all individuals: 109
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 526
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variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 2.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.401e0

VQSLOD
type: SiteQuality
SIO_000300: -6.853e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.68e-1

DP
type: SiteQuality
SIO_000300: 2.448778e6

FS
type: SiteQuality
SIO_000300: 1.364e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

QD
type: SiteQuality
SIO_000300: 8.880000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 3.88e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

GenotypeDepth
all individuals: 1451
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8242
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 21738
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variant carriers: 1

GenotypeQuality
all individuals: 3515
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

FS
type: SiteQuality
SIO_000300: 2.741e0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.446009e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.357e1

GenotypeDepth
all individuals: 584
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 982
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
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GenotypeQuality
all individuals: 9195
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GenotypeQuality
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GenotypeQuality
all individuals: 23
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 588
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variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 4.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.97e-1

QD
type: SiteQuality
SIO_000300: 1.485e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

DP
type: SiteQuality
SIO_000300: 2.444262e6

VQSLOD
type: SiteQuality
SIO_000300: 8.599999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 9.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.56e-1

GenotypeDepth
all individuals: 829
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3816
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variant carriers: 0

GenotypeDepth
all individuals: 241
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GenotypeDepth
all individuals: 584
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1044
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004988280545706e-5
allele num: 66556
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

QD
type: SiteQuality
SIO_000300: 8.619999999999999e0

FS
type: SiteQuality
SIO_000300: 2.128e0

DP
type: SiteQuality
SIO_000300: 2.439465e6

VQSLOD
type: SiteQuality
SIO_000300: -9.59e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.709e0

GenotypeDepth
all individuals: 789
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variant carriers: 3

GenotypeDepth
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variant carriers: 10

GenotypeDepth
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variant carriers: 19

GenotypeDepth
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variant carriers: 8

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 600
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GenotypeQuality
all individuals: 4723
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GenotypeQuality
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GenotypeQuality
all individuals: 31
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 231
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GenotypeQuality
all individuals: 21832
bin: 9.75e1
variant carriers: 109

GenotypeQuality
all individuals: 5329
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 95
allele frequency: 1.427927250864272e-3
allele num: 66530
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.114711997064938e-5
allele num: 16354
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 4.81139337952271e-4
allele num: 10392
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 8
allele frequency: 6.932409012131716e-4
allele num: 11540
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

DP
type: SiteQuality
SIO_000300: 2.437979e6

QD
type: SiteQuality
SIO_000300: 1.444e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.24e0

MQRankSum
type: SiteQuality
SIO_000300: 8.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-2

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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GenotypeDepth
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variant carriers: 8

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 58

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5253
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GenotypeQuality
all individuals: 3953
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variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.92492781520693e-4
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 295
allele frequency: 4.432224525977343e-3
allele num: 66558
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 42
allele frequency: 6.355932203389831e-3
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.106497313141182e-5
allele num: 16376
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.600104004160167e-4
allele num: 11538
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

BaseQRankSum
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SIO_000300: -2.122e0

MQ
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SIO_000300: 5.859e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-1

DP
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SIO_000300: 2.435025e6

VQSLOD
type: SiteQuality
SIO_000300: 7.33e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 1.297e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 429
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508113651444773e-5
allele num: 66308
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.692e0

FS
type: SiteQuality
SIO_000300: 5.545e0

MQRankSum
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SIO_000300: -2.44e0

ClippingRankSum
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SIO_000300: 1.15e0

VQSLOD
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SIO_000300: -2.983e0

DP
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SIO_000300: 5.522805e6

InbreedingCoeff
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SIO_000300: 3.7e-3

MQ
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SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.563e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 271
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508068164681044e-5
allele num: 66310
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

BaseQRankSum
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SIO_000300: -9.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.935e0

FS
type: SiteQuality
SIO_000300: 1.609e0

VQSLOD
type: SiteQuality
SIO_000300: -2.199e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

DP
type: SiteQuality
SIO_000300: 5.523238e6

QD
type: SiteQuality
SIO_000300: 1.806e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e0

GenotypeDepth
all individuals: 147
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 232
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66310
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 5.523362e6

QD
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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MQ
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SIO_000300: 5.529e1

MQRankSum
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SIO_000300: -5.298e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 4074
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508068164681044e-5
allele num: 66310
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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DP
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ReadPosRankSum
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SIO_000300: 1.65e0

ClippingRankSum
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SIO_000300: -1.695e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 250
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.508022680661117e-5
allele num: 66312
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

FS
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InbreedingCoeff
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SIO_000300: 9.599999999999999e-3

QD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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MQ
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SIO_000300: 5.984e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66314
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.352e1

DP
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SIO_000300: 5.523565e6

ClippingRankSum
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SIO_000300: 1.01e0

FS
type: SiteQuality
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ReadPosRankSum
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QD
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MQRankSum
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SIO_000300: -4.74e-1

BaseQRankSum
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SIO_000300: -1.423e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.195e-1

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

East Asian
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allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66312
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.523385e6

FS
type: SiteQuality
SIO_000300: 1.646e0

VQSLOD
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SIO_000300: -1.524e0

MQRankSum
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QD
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MQ
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SIO_000300: 5.884e1

ClippingRankSum
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SIO_000300: 4.39e-1

InbreedingCoeff
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SIO_000300: 4.2e-3

BaseQRankSum
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SIO_000300: 7.9e0

ReadPosRankSum
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SIO_000300: -8.2e-1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508022680661117e-5
allele num: 66312
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.77e-1

InbreedingCoeff
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SIO_000300: 4.3e-3

BaseQRankSum
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SIO_000300: -1.879e0

DP
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SIO_000300: 5.523367e6

MQRankSum
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SIO_000300: 9.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.33e-1

QD
type: SiteQuality
SIO_000300: 1.286e1

MQ
type: SiteQuality
SIO_000300: 5.93e1

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 15

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 1.295784381478922e-3
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66310
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.735e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.23e-1

FS
type: SiteQuality
SIO_000300: 7.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.004e1

VQSLOD
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SIO_000300: 2.28e0

DP
type: SiteQuality
SIO_000300: 5.523606e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.016136329362087e-5
allele num: 66310
num of homozygotes: 0

InbreedingCoeff
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DP
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QD
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MQ
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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FS
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele num: 16512
num of homozygotes: 0

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

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

Other
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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FS
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QD
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InbreedingCoeff
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.269558769002595e-5
allele num: 10788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13472
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: 2
allele frequency: 3.192746080904186e-5
allele num: 62642
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e0

QD
type: SiteQuality
SIO_000300: 1.716e1

MQRankSum
type: SiteQuality
SIO_000300: 4.42e-1

DP
type: SiteQuality
SIO_000300: 1.183235e6

MQ
type: SiteQuality
SIO_000300: 5.47e1

FS
type: SiteQuality
SIO_000300: 7.466e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.344e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

GenotypeDepth
all individuals: 406
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2182
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14493
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 24
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 47
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1612
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 297
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5260
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19734
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3632
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3425
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2770
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6017
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4393
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3227
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6235
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
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: 13526
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.620564808110065e-4
allele num: 8286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10808
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

MQ
type: SiteQuality
SIO_000300: 5.545e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.345e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.475e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.81e-1

QD
type: SiteQuality
SIO_000300: 1.288e1

DP
type: SiteQuality
SIO_000300: 1.196595e6

GenotypeDepth
all individuals: 3736
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 405
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10140
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26872
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2346
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3462
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31809
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4411
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 522
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4417
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 405
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1840
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4375
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2358
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.007455168245013e-4
allele num: 9926
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13714
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.77e0