21-39817403-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817403
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817403
    reference: chr 21
allele count: 3
allele frequency: 2.473533194815474e-5
allele num: 121284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.181C>G
  hgvsp: ENSP00000394694.1:p.Gln61Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.181C>G
  hgvsp: ENSP00000381881.1:p.Gln61Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.181C>G
  hgvsp: ENSP00000414150.2:p.Gln61Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.160C>G
  hgvsp: ENSP00000381879.1:p.Gln54Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.331C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.181C>G
  hgvsp: ENSP00000381891.2:p.Gln61Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.367C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.142C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.160C>G
  hgvsp: ENSP00000288319.7:p.Gln54Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.160C>G
  hgvsp: ENSP00000415659.2:p.Gln54Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.226C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.160C>G
  hgvsp: ENSP00000381877.1:p.Gln54Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21920C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21920C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.181C>G
  hgvsp: ENSP00000381882.1:p.Gln61Glu
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln61Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

21-39817407-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817407
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817407
    reference: chr 21
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.156T>C
  hgvsp: ENST00000429727.2:c.156T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.156T>C
  hgvsp: ENST00000398907.1:c.156T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21924T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.177T>C
  hgvsp: ENST00000398911.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.156T>C
  hgvsp: ENST00000398905.1:c.156T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.156T>C
  hgvsp: ENST00000288319.7:c.156T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.177T>C
  hgvsp: ENST00000442448.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.138T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21924T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.177T>C
  hgvsp: ENST00000417133.2:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.177T>C
  hgvsp: ENST00000398910.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.222T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.327T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.177T>C
  hgvsp: ENST00000398919.2:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.363T>C
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13389
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro59Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

21-39817412-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817412
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817412
    reference: chr 21
allele count: 5
allele frequency: 4.121875618281343e-5
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.172G>A
  hgvsp: ENSP00000381891.2:p.Val58Ile
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.217G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.172G>A
  hgvsp: ENSP00000381882.1:p.Val58Ile
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.151G>A
  hgvsp: ENSP00000381879.1:p.Val51Ile
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.133G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.151G>A
  hgvsp: ENSP00000415659.2:p.Val51Ile
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.172G>A
  hgvsp: ENSP00000414150.2:p.Val58Ile
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.358G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21929G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.172G>A
  hgvsp: ENSP00000394694.1:p.Val58Ile
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.151G>A
  hgvsp: ENSP00000381877.1:p.Val51Ile
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.151G>A
  hgvsp: ENSP00000288319.7:p.Val51Ile
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21929G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.322G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.172G>A
  hgvsp: ENSP00000381881.1:p.Val58Ile
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val58Ile
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

21-39817414-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817414
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817414
    reference: chr 21
allele count: 3
allele frequency: 2.472962279082036e-5
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.149G>A
  hgvsp: ENSP00000381877.1:p.Arg50His
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.170G>A
  hgvsp: ENSP00000381881.1:p.Arg57His
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.170G>A
  hgvsp: ENSP00000414150.2:p.Arg57His
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.149G>A
  hgvsp: ENSP00000288319.7:p.Arg50His
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.170G>A
  hgvsp: ENSP00000381891.2:p.Arg57His
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.356G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.149G>A
  hgvsp: ENSP00000381879.1:p.Arg50His
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.170G>A
  hgvsp: ENSP00000394694.1:p.Arg57His
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.149G>A
  hgvsp: ENSP00000415659.2:p.Arg50His
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.320G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.131G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.170G>A
  hgvsp: ENSP00000381882.1:p.Arg57His
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.215G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21931G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21931G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg57His
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

21-39817415-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817415
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817415
    reference: chr 21
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21932C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.169C>T
  hgvsp: ENSP00000394694.1:p.Arg57Cys
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.355C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.169C>T
  hgvsp: ENSP00000381881.1:p.Arg57Cys
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.319C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.169C>T
  hgvsp: ENSP00000381891.2:p.Arg57Cys
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.214C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.169C>T
  hgvsp: ENSP00000381882.1:p.Arg57Cys
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.148C>T
  hgvsp: ENSP00000288319.7:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.148C>T
  hgvsp: ENSP00000381879.1:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.148C>T
  hgvsp: ENSP00000415659.2:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.148C>T
  hgvsp: ENSP00000381877.1:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.130C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21932C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.169C>T
  hgvsp: ENSP00000414150.2:p.Arg57Cys
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg57Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ

21-39817419-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817419
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817419
    reference: chr 21
allele count: 6
allele frequency: 4.945679948564928e-5
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.144C>T
  hgvsp: ENST00000429727.2:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21936C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.165C>T
  hgvsp: ENST00000417133.2:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.144C>T
  hgvsp: ENST00000398907.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.126C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.315C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.351C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.144C>T
  hgvsp: ENST00000398905.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.165C>T
  hgvsp: ENST00000398911.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.165C>T
  hgvsp: ENST00000398910.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.144C>T
  hgvsp: ENST00000288319.7:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.165C>T
  hgvsp: ENST00000442448.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.165C>T
  hgvsp: ENST00000398919.2:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.210C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21936C>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser55Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

21-39817437-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817437
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817437
    reference: chr 21
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.126A>G
  hgvsp: ENST00000288319.7:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.147A>G
  hgvsp: ENST00000398910.1:c.147A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.126A>G
  hgvsp: ENST00000398907.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.126A>G
  hgvsp: ENST00000398905.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.108A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.192A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.147A>G
  hgvsp: ENST00000442448.1:c.147A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.126A>G
  hgvsp: ENST00000429727.2:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.333A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.147A>G
  hgvsp: ENST00000398911.1:c.147A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.147A>G
  hgvsp: ENST00000417133.2:c.147A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.297A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21954A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.147A>G
  hgvsp: ENST00000398919.2:c.147A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21954A>G
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly49Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

21-39817438-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817438
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817438
    reference: chr 21
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.146G>A
  hgvsp: ENSP00000394694.1:p.Gly49Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21955G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.146G>A
  hgvsp: ENSP00000381882.1:p.Gly49Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.125G>A
  hgvsp: ENSP00000288319.7:p.Gly42Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.125G>A
  hgvsp: ENSP00000415659.2:p.Gly42Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.146G>A
  hgvsp: ENSP00000414150.2:p.Gly49Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.146G>A
  hgvsp: ENSP00000381891.2:p.Gly49Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.296G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.125G>A
  hgvsp: ENSP00000381877.1:p.Gly42Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21955G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.125G>A
  hgvsp: ENSP00000381879.1:p.Gly42Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.191G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.146G>A
  hgvsp: ENSP00000381881.1:p.Gly49Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.107G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.332G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly49Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

21-39817445-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817445
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817445
    reference: chr 21
allele count: 2
allele frequency: 1.648532805802836e-5
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.100G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.118G>A
  hgvsp: ENSP00000381879.1:p.Asp40Asn
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.139G>A
  hgvsp: ENSP00000381891.2:p.Asp47Asn
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.139G>A
  hgvsp: ENSP00000381882.1:p.Asp47Asn
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.139G>A
  hgvsp: ENSP00000381881.1:p.Asp47Asn
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.118G>A
  hgvsp: ENSP00000381877.1:p.Asp40Asn
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21962G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.139G>A
  hgvsp: ENSP00000414150.2:p.Asp47Asn
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.289G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.139G>A
  hgvsp: ENSP00000394694.1:p.Asp47Asn
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21962G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.118G>A
  hgvsp: ENSP00000415659.2:p.Asp40Asn
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.325G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.184G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.118G>A
  hgvsp: ENSP00000288319.7:p.Asp40Asn
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp47Asn
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

21-39817446-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817446
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817446
    reference: chr 21
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.117C>T
  hgvsp: ENST00000398905.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.117C>T
  hgvsp: ENST00000429727.2:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.138C>T
  hgvsp: ENST00000442448.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.138C>T
  hgvsp: ENST00000398919.2:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.138C>T
  hgvsp: ENST00000398910.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21963C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21963C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.138C>T
  hgvsp: ENST00000398911.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.117C>T
  hgvsp: ENST00000288319.7:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.138C>T
  hgvsp: ENST00000417133.2:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.117C>T
  hgvsp: ENST00000398907.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.288C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.99C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.324C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.183C>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser46Ser
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: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

21-39817450-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817450
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817450
    reference: chr 21
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.113C>T
  hgvsp: ENSP00000288319.7:p.Ser38Phe
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.95C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21967C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.320C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.113C>T
  hgvsp: ENSP00000415659.2:p.Ser38Phe
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.134C>T
  hgvsp: ENSP00000394694.1:p.Ser45Phe
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.113C>T
  hgvsp: ENSP00000381877.1:p.Ser38Phe
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.134C>T
  hgvsp: ENSP00000414150.2:p.Ser45Phe
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.179C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.113C>T
  hgvsp: ENSP00000381879.1:p.Ser38Phe
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.134C>T
  hgvsp: ENSP00000381891.2:p.Ser45Phe
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.134C>T
  hgvsp: ENSP00000381882.1:p.Ser45Phe
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21967C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.284C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.134C>T
  hgvsp: ENSP00000381881.1:p.Ser45Phe
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser45Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

21-39817458-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817458
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817458
    reference: chr 21
allele count: 2
allele frequency: 1.648559982854976e-5
allele num: 121318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.105G>A
  hgvsp: ENST00000288319.7:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.276G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.87G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.126G>A
  hgvsp: ENST00000417133.2:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.105G>A
  hgvsp: ENST00000398907.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.126G>A
  hgvsp: ENST00000398911.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.126G>A
  hgvsp: ENST00000398910.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.171G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21975G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.105G>A
  hgvsp: ENST00000398905.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21975G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.105G>A
  hgvsp: ENST00000429727.2:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.126G>A
  hgvsp: ENST00000442448.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.312G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.126G>A
  hgvsp: ENST00000398919.2:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala42Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

21-39817460-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817460
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817460
    reference: chr 21
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.274G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.124G>A
  hgvsp: ENSP00000414150.2:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.124G>A
  hgvsp: ENSP00000381881.1:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.124G>A
  hgvsp: ENSP00000381891.2:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.103G>A
  hgvsp: ENSP00000381877.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21977G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.124G>A
  hgvsp: ENSP00000394694.1:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.310G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21977G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.103G>A
  hgvsp: ENSP00000381879.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.85G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.103G>A
  hgvsp: ENSP00000288319.7:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.103G>A
  hgvsp: ENSP00000415659.2:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.124G>A
  hgvsp: ENSP00000381882.1:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.169G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala42Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

21-39817461-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817461
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817461
    reference: chr 21
allele count: 4
allele frequency: 3.297283038776049e-5
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.123C>T
  hgvsp: ENST00000398910.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.123C>T
  hgvsp: ENST00000442448.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21978C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.309C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.84C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.123C>T
  hgvsp: ENST00000398919.2:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.273C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.123C>T
  hgvsp: ENST00000398911.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.102C>T
  hgvsp: ENST00000288319.7:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.102C>T
  hgvsp: ENST00000398905.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.123C>T
  hgvsp: ENST00000417133.2:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.102C>T
  hgvsp: ENST00000429727.2:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21978C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.102C>T
  hgvsp: ENST00000398907.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.168C>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr41Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

21-39817461-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817461
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817461
    reference: chr 21
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21978C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.102C>G
  hgvsp: ENST00000398907.1:c.102C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.123C>G
  hgvsp: ENST00000442448.1:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.123C>G
  hgvsp: ENST00000398910.1:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.102C>G
  hgvsp: ENST00000429727.2:c.102C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.84C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.123C>G
  hgvsp: ENST00000417133.2:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.309C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.102C>G
  hgvsp: ENST00000288319.7:c.102C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.273C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.123C>G
  hgvsp: ENST00000398919.2:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.123C>G
  hgvsp: ENST00000398911.1:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21978C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.102C>G
  hgvsp: ENST00000398905.1:c.102C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.168C>G
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr41Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

21-39817475-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817475
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817475
    reference: chr 21
allele count: 2
allele frequency: 1.648750247312537e-5
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.88A>G
  hgvsp: ENSP00000288319.7:p.Lys30Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.88A>G
  hgvsp: ENSP00000381879.1:p.Lys30Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.109A>G
  hgvsp: ENSP00000394694.1:p.Lys37Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.88A>G
  hgvsp: ENSP00000381877.1:p.Lys30Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.109A>G
  hgvsp: ENSP00000381881.1:p.Lys37Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.109A>G
  hgvsp: ENSP00000381891.2:p.Lys37Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21992A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.88A>G
  hgvsp: ENSP00000415659.2:p.Lys30Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.109A>G
  hgvsp: ENSP00000414150.2:p.Lys37Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.259A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21992A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.154A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.109A>G
  hgvsp: ENSP00000381882.1:p.Lys37Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.295A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.70A>G
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys37Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

21-39817478-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817478
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817478
    reference: chr 21
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-21995G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.106G>A
  hgvsp: ENSP00000381882.1:p.Ala36Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.106G>A
  hgvsp: ENSP00000414150.2:p.Ala36Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.106G>A
  hgvsp: ENSP00000381881.1:p.Ala36Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.85G>A
  hgvsp: ENSP00000288319.7:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.85G>A
  hgvsp: ENSP00000381877.1:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.85G>A
  hgvsp: ENSP00000415659.2:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.67G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.85G>A
  hgvsp: ENSP00000381879.1:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.106G>A
  hgvsp: ENSP00000394694.1:p.Ala36Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.106G>A
  hgvsp: ENSP00000381891.2:p.Ala36Thr
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-21995G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.256G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.292G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.151G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala36Thr
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

21-39817483-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817483
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817483
    reference: chr 21
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.101A>C
  hgvsp: ENSP00000394694.1:p.His34Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.101A>C
  hgvsp: ENSP00000381881.1:p.His34Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.101A>C
  hgvsp: ENSP00000381882.1:p.His34Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.101A>C
  hgvsp: ENSP00000381891.2:p.His34Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22000A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.80A>C
  hgvsp: ENSP00000288319.7:p.His27Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.101A>C
  hgvsp: ENSP00000414150.2:p.His34Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.287A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.80A>C
  hgvsp: ENSP00000381879.1:p.His27Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.146A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.62A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.80A>C
  hgvsp: ENSP00000415659.2:p.His27Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.80A>C
  hgvsp: ENSP00000381877.1:p.His27Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22000A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.251A>C
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His34Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS

21-39817488-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817488
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817488
    reference: chr 21
allele count: 6
allele frequency: 4.947392724034434e-5
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.246G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22005G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.75G>A
  hgvsp: ENST00000288319.7:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.75G>A
  hgvsp: ENST00000429727.2:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.282G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22005G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.96G>A
  hgvsp: ENST00000398919.2:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.96G>A
  hgvsp: ENST00000398911.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.57G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.96G>A
  hgvsp: ENST00000442448.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.75G>A
  hgvsp: ENST00000398907.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.96G>A
  hgvsp: ENST00000417133.2:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.96G>A
  hgvsp: ENST00000398910.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.141G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.75G>A
  hgvsp: ENST00000398905.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr32Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

21-39817489-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817489
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817489
    reference: chr 21
allele count: 3
allele frequency: 2.473777953690877e-5
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.56C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.281C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.74C>T
  hgvsp: ENSP00000415659.2:p.Thr25Met
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.95C>T
  hgvsp: ENSP00000394694.1:p.Thr32Met
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.140C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.74C>T
  hgvsp: ENSP00000381879.1:p.Thr25Met
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22006C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.95C>T
  hgvsp: ENSP00000381891.2:p.Thr32Met
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.245C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.95C>T
  hgvsp: ENSP00000381882.1:p.Thr32Met
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.74C>T
  hgvsp: ENSP00000288319.7:p.Thr25Met
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.74C>T
  hgvsp: ENSP00000381877.1:p.Thr25Met
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22006C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.95C>T
  hgvsp: ENSP00000381881.1:p.Thr32Met
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.95C>T
  hgvsp: ENSP00000414150.2:p.Thr32Met
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr32Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

21-39817490-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817490
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817490
    reference: chr 21
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.94A>G
  hgvsp: ENSP00000381891.2:p.Thr32Ala
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.94A>G
  hgvsp: ENSP00000381882.1:p.Thr32Ala
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.73A>G
  hgvsp: ENSP00000381877.1:p.Thr25Ala
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.244A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.73A>G
  hgvsp: ENSP00000415659.2:p.Thr25Ala
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.73A>G
  hgvsp: ENSP00000381879.1:p.Thr25Ala
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.73A>G
  hgvsp: ENSP00000288319.7:p.Thr25Ala
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.94A>G
  hgvsp: ENSP00000414150.2:p.Thr32Ala
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.94A>G
  hgvsp: ENSP00000394694.1:p.Thr32Ala
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.280A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.94A>G
  hgvsp: ENSP00000381881.1:p.Thr32Ala
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.139A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.55A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22007A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22007A>G
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr32Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

21-39817491-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817491
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817491
    reference: chr 21
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.243A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.93A>T
  hgvsp: ENST00000417133.2:c.93A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22008A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.72A>T
  hgvsp: ENST00000398907.1:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.93A>T
  hgvsp: ENST00000442448.1:c.93A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.93A>T
  hgvsp: ENST00000398919.2:c.93A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.93A>T
  hgvsp: ENST00000398910.1:c.93A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.72A>T
  hgvsp: ENST00000288319.7:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.72A>T
  hgvsp: ENST00000398905.1:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.72A>T
  hgvsp: ENST00000429727.2:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.138A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.279A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.93A>T
  hgvsp: ENST00000398911.1:c.93A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22008A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.54A>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly31Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

21-39817493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817493
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817493
    reference: chr 21
allele count: 2
allele frequency: 1.649375711293276e-5
allele num: 121258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.52G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.91G>A
  hgvsp: ENSP00000381882.1:p.Gly31Arg
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22010G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.70G>A
  hgvsp: ENSP00000288319.7:p.Gly24Arg
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.70G>A
  hgvsp: ENSP00000381879.1:p.Gly24Arg
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.70G>A
  hgvsp: ENSP00000415659.2:p.Gly24Arg
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.241G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.91G>A
  hgvsp: ENSP00000394694.1:p.Gly31Arg
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.91G>A
  hgvsp: ENSP00000381881.1:p.Gly31Arg
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.277G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.91G>A
  hgvsp: ENSP00000414150.2:p.Gly31Arg
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.70G>A
  hgvsp: ENSP00000381877.1:p.Gly24Arg
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.91G>A
  hgvsp: ENSP00000381891.2:p.Gly31Arg
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.136G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22010G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 40794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly31Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

21-39817494-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817494
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817494
    reference: chr 21
allele count: 7
allele frequency: 5.772434153018983e-5
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22011C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.90C>T
  hgvsp: ENST00000398911.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.90C>T
  hgvsp: ENST00000417133.2:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.69C>T
  hgvsp: ENST00000288319.7:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.69C>T
  hgvsp: ENST00000429727.2:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.90C>T
  hgvsp: ENST00000442448.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.69C>T
  hgvsp: ENST00000398905.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.90C>T
  hgvsp: ENST00000398910.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.90C>T
  hgvsp: ENST00000398919.2:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.135C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.51C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.69C>T
  hgvsp: ENST00000398907.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.276C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.240C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22011C>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13822
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40782
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr30Tyr
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

21-39817499-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817499
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817499
    reference: chr 21
allele count: 2
allele frequency: 1.649566164098842e-5
allele num: 121244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.271G>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.85G>C
  hgvsp: ENSP00000381891.2:p.Ala29Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.64G>C
  hgvsp: ENSP00000288319.7:p.Ala22Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.85G>C
  hgvsp: ENSP00000414150.2:p.Ala29Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.64G>C
  hgvsp: ENSP00000381879.1:p.Ala22Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.85G>C
  hgvsp: ENSP00000394694.1:p.Ala29Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.235G>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22016G>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.64G>C
  hgvsp: ENSP00000415659.2:p.Ala22Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.85G>C
  hgvsp: ENSP00000381882.1:p.Ala29Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.64G>C
  hgvsp: ENSP00000381877.1:p.Ala22Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.130G>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.46G>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.85G>C
  hgvsp: ENSP00000381881.1:p.Ala29Pro
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22016G>C
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala29Pro
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/21-39817506-AAAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817506
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817503
    reference: chr 21
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.54_56delGTT
  hgvsp: ENSP00000288319.7:p.Leu18del
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.75_77delGTT
  hgvsp: ENSP00000381882.1:p.Leu25del
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.54_56delGTT
  hgvsp: ENSP00000381879.1:p.Leu18del
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.54_56delGTT
  hgvsp: ENSP00000381877.1:p.Leu18del
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.75_77delGTT
  hgvsp: ENSP00000414150.2:p.Leu25del
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22026_-40-22024delGTT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.36_38delGTT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.225_227delGTT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.261_263delGTT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.54_56delGTT
  hgvsp: ENSP00000415659.2:p.Leu18del
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.75_77delGTT
  hgvsp: ENSP00000394694.1:p.Leu25del
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.75_77delGTT
  hgvsp: ENSP00000381891.2:p.Leu25del
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.120_122delGTT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.75_77delGTT
  hgvsp: ENSP00000381881.1:p.Leu25del
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22026_-40-22024delGTT
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu25del
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: AAAC
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

21-39817512-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817512
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817512
    reference: chr 21
allele count: 3
allele frequency: 2.475778632379884e-5
allele num: 121174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.72G>A
  hgvsp: ENST00000442448.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.51G>A
  hgvsp: ENST00000429727.2:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.258G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.72G>A
  hgvsp: ENST00000398919.2:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.51G>A
  hgvsp: ENST00000398907.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.72G>A
  hgvsp: ENST00000417133.2:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.117G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.51G>A
  hgvsp: ENST00000398905.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.72G>A
  hgvsp: ENST00000398910.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22029G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.51G>A
  hgvsp: ENST00000288319.7:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.72G>A
  hgvsp: ENST00000398911.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22029G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.222G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.33G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser24Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

21-39817513-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817513
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817513
    reference: chr 21
allele count: 1
allele frequency: 8.253412786187088e-6
allele num: 121162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.221C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.71C>T
  hgvsp: ENSP00000381881.1:p.Ser24Leu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.50C>T
  hgvsp: ENSP00000381877.1:p.Ser17Leu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.116C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22030C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22030C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.32C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.71C>T
  hgvsp: ENSP00000414150.2:p.Ser24Leu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.71C>T
  hgvsp: ENSP00000394694.1:p.Ser24Leu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.50C>T
  hgvsp: ENSP00000415659.2:p.Ser17Leu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.50C>T
  hgvsp: ENSP00000381879.1:p.Ser17Leu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.50C>T
  hgvsp: ENSP00000288319.7:p.Ser17Leu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.257C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.71C>T
  hgvsp: ENSP00000381891.2:p.Ser24Leu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.71C>T
  hgvsp: ENSP00000381882.1:p.Ser24Leu
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40670
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser24Leu
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

21-39817517-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817517
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817517
    reference: chr 21
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.217C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22034C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.46C>G
  hgvsp: ENSP00000381879.1:p.Gln16Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.46C>G
  hgvsp: ENSP00000381877.1:p.Gln16Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.67C>G
  hgvsp: ENSP00000381891.2:p.Gln23Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.46C>G
  hgvsp: ENSP00000288319.7:p.Gln16Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22034C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.67C>G
  hgvsp: ENSP00000394694.1:p.Gln23Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.67C>G
  hgvsp: ENSP00000381881.1:p.Gln23Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.67C>G
  hgvsp: ENSP00000381882.1:p.Gln23Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.46C>G
  hgvsp: ENSP00000415659.2:p.Gln16Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.112C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.253C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.67C>G
  hgvsp: ENSP00000414150.2:p.Gln23Glu
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.28C>G
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln23Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum

21-39817521-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817521
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817521
    reference: chr 21
allele count: 2
allele frequency: 1.651991475723985e-5
allele num: 121066
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.42G>A
  hgvsp: ENST00000288319.7:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.213G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.249G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.63G>A
  hgvsp: ENST00000417133.2:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.42G>A
  hgvsp: ENST00000398907.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22038G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.42G>A
  hgvsp: ENST00000398905.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.63G>A
  hgvsp: ENST00000398910.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000492833
  gene symbol: ERG
  hgvsc: ENST00000492833.1:n.24G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.63G>A
  hgvsp: ENST00000442448.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.42G>A
  hgvsp: ENST00000429727.2:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.63G>A
  hgvsp: ENST00000398919.2:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.108G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22038G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.63G>A
  hgvsp: ENST00000398911.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu21Glu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

21-39817556-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817556
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817556
    reference: chr 21
allele count: 1
allele frequency: 8.430423713095819e-6
allele num: 118618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-12T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22073T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-12T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-12T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-12T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.85-12T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-12T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-12T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-12T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-12T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-12T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-12T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-12T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22073T>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

21-39817564-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817564
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817564
    reference: chr 21
allele count: 1
allele frequency: 8.522388314101144e-6
allele num: 117338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22081G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-20G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-20G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-20G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-20G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-20G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-20G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-20G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-20G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-20G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.85-20G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-20G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22081G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-20G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

21-39817566-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817566
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817566
    reference: chr 21
allele count: 3
allele frequency: 2.561912894961571e-5
allele num: 117100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-22A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-22A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22083A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-22A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22083A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-22A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-22A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-22A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-22A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-22A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-22A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-22A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-22A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.85-22A>C
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27989
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10041
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

21-39817573-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817573
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817573
    reference: chr 21
allele count: 1
allele frequency: 8.597269507204511e-6
allele num: 116316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-29T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-29T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-29T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22090T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-29T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.85-29T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22090T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-29T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-29T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-29T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-29T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-29T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-29T>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-29T>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13676
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

21-39817576-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817576
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817576
    reference: chr 21
allele count: 1
allele frequency: 8.629616845012081e-6
allele num: 115880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-32G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22093G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-32G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-32G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-32G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.85-32G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-32G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-32G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-32G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-32G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-32G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22093G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-32G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-32G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

21-39817582-AACAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817582
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817578
    reference: chr 21
allele count: 8
allele frequency: 6.960758722700774e-5
allele num: 114930
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-42_40-39delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-42_40-39delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-42_19-39delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22103_-40-22100delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-42_226-39delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-42_40-39delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-42_190-39delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22103_-40-22100delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.85-42_85-39delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-42_40-39delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-42_40-39delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-42_19-39delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-42_19-39delCTGT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-42_19-39delCTGT
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15232
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14829
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7363
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15347
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: AACAG
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/21-39817585-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817585
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817585
    reference: chr 21
allele count: 4
allele frequency: 3.504038404260911e-5
allele num: 114154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-41T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22102T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-41T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-41T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-41T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-41T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.85-41T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-41T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-41T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-41T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-41T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22102T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-41T>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-41T>G
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17288
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

21-39817588-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39817588
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39817588
    reference: chr 21
allele count: 7
allele frequency: 6.199188791866665e-5
allele num: 112918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-44G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-44G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-22105G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-44G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-44G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-44G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-44G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000473107
  gene symbol: ERG
  hgvsc: ENST00000473107.1:n.85-44G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-44G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-22105G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-44G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-44G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-44G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-44G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17740
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14234
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/21-39822770-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39822770
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39822769
    reference: chr 21
allele count: 10
allele frequency: 7.115411982353779e-4
allele num: 14054
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27288delT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5227delT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5227delT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5227delT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5227delT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5227delT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5227delT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5227delT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5227delT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5227delT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27288delT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5227delT
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5227delT
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: CA
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

21-39822777-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39822777
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39822777
    reference: chr 21
allele count: 19
allele frequency: 1.335770528683915e-3
allele num: 14224
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5233A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27294A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5233A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27294A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5233A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5233A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5233A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5233A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5233A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5233A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5233A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5233A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5233A>G
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 2
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

21-39822803-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39822803
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39822803
    reference: chr 21
allele count: 1
allele frequency: 6.657789613848202e-5
allele num: 15020
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5259T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5259T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5259T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5259T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5259T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5259T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5259T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5259T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5259T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5259T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5259T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27320T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27320T>C
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

21-39822818-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39822818
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39822818
    reference: chr 21
allele count: 1
allele frequency: 6.510416666666667e-5
allele num: 15360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5274G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27335G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5274G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27335G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5274G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5274G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5274G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5274G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5274G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5274G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5274G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5274G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5274G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

21-39822851-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39822851
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39822851
    reference: chr 21
allele count: 1
allele frequency: 6.384065372829418e-5
allele num: 15664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5307G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5307G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5307G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5307G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5307G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5307G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5307G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27368G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27368G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5307G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5307G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5307G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5307G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

21-39823066-GTA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823066
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823064
    reference: chr 21
allele count: 0
allele frequency: 0.0e0
allele num: 57168
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5524_40-5523delTA
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5524_19-5523delTA
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5524_190-5523delTA
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5524_40-5523delTA
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5524_19-5523delTA
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5524_226-5523delTA
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27585_-40-27584delTA
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5524_19-5523delTA
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5524_40-5523delTA
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5524_40-5523delTA
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5524_19-5523delTA
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27585_-40-27584delTA
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5524_40-5523delTA
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: GTA
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

21-39823067-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823067
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823067
    reference: chr 21
allele count: 985
allele frequency: 2.995013378739966e-2
allele num: 32888
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27584A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27584A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5523A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5523A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5523A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5523A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5523A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5523A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5523A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5523A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5523A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5523A>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5523A>C
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 1.75e1
  variant carriers: 186
genotype depth: GenotypeDepth
  all individuals: 13200
  bin: 1.25e1
  variant carriers: 322
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 24219
  bin: 7.5e0
  variant carriers: 191
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 3.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 6909
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 2.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

21-39823068-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823068
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823068
    reference: chr 21
allele count: 1
allele frequency: 1.977691638319753e-5
allele num: 50564
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5524T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5524T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5524T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5524T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5524T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5524T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5524T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5524T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27585T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5524T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27585T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5524T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5524T>C
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6979
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13405
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum

21-39823069-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823069
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823069
    reference: chr 21
allele count: 2
allele frequency: 3.903810118675827e-5
allele num: 51232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5525C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5525C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5525C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5525C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5525C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5525C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5525C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5525C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27586C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5525C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5525C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27586C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5525C>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13351
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23999
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7044
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

21-39823070-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823070
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823070
    reference: chr 21
allele count: 0
allele frequency: 0.0e0
allele num: 51098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5526T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5526T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5526T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5526T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5526T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5526T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5526T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5526T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27587T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5526T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5526T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27587T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5526T>C
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7005
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24019
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

21-39823072-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823072
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823072
    reference: chr 21
allele count: 0
allele frequency: 0.0e0
allele num: 51356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5528C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5528C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5528C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5528C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5528C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27589C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5528C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27589C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5528C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5528C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5528C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5528C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5528C>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24175
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP

21-39823074-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823074
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823074
    reference: chr 21
allele count: 14
allele frequency: 2.75178866263071e-4
allele num: 50876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27591T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5530T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5530T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5530T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5530T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5530T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5530T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5530T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5530T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5530T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5530T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5530T>C
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27591T>C
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13334
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24287
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

21-39823076-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823076
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823076
    reference: chr 21
allele count: 1
allele frequency: 1.932740626207963e-5
allele num: 51740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5532C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5532C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5532C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27593C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5532C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27593C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5532C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5532C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5532C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5532C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5532C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5532C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5532C>G
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13266
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

21-39823089-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823089
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823089
    reference: chr 21
allele count: 1
allele frequency: 1.886792452830189e-5
allele num: 53000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27606C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5545C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27606C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5545C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5545C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5545C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5545C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5545C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5545C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5545C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5545C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5545C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5545C>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12498
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25672
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

21-39823096-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823096
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823096
    reference: chr 21
allele count: 0
allele frequency: 0.0e0
allele num: 54026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5552C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5552C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5552C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5552C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5552C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5552C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5552C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5552C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27613C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5552C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5552C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27613C>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5552C>G
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25835
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS

21-39823099-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823099
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823099
    reference: chr 21
allele count: 1
allele frequency: 1.827351801768876e-5
allele num: 54724
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5555A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27616A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5555A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5555A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5555A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5555A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5555A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5555A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5555A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27616A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5555A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5555A>G
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5555A>G
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

21-39823102-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823102
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823102
    reference: chr 21
allele count: 4
allele frequency: 7.247689798876609e-5
allele num: 55190
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5558C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5558C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5558C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5558C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5558C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5558C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27619C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5558C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5558C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5558C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5558C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5558C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27619C>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25853
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10960
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8391
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

21-39823107-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823107
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823107
    reference: chr 21
allele count: 1
allele frequency: 1.779676098949991e-5
allele num: 56190
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5563G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27624G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5563G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5563G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5563G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5563G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5563G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5563G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5563G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5563G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5563G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5563G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27624G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25525
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10500
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

21-39823109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823109
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823109
    reference: chr 21
allele count: 4
allele frequency: 7.053429730206313e-5
allele num: 56710
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5565C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5565C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5565C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27626C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5565C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5565C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5565C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27626C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5565C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5565C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5565C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5565C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5565C>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25389
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

21-39823124-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823124
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823124
    reference: chr 21
allele count: 4
allele frequency: 6.759725555142461e-5
allele num: 59174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5580C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27641C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5580C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27641C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5580C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5580C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5580C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5580C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5580C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5580C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5580C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5580C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5580C>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9789
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

21-39823147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823147
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823147
    reference: chr 21
allele count: 1
allele frequency: 1.694226077527785e-5
allele num: 59024
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5603C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5603C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5603C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5603C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5603C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5603C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5603C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5603C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5603C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27664C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5603C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5603C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27664C>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

21-39823152-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823152
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823152
    reference: chr 21
allele count: 1
allele frequency: 1.703171304969854e-5
allele num: 58714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5608G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5608G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5608G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27669G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5608G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5608G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5608G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5608G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27669G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5608G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5608G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5608G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5608G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

21-39823153-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823153
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823153
    reference: chr 21
allele count: 77
allele frequency: 1.315969373803664e-3
allele num: 58512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5609C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5609C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5609C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27670C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5609C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5609C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5609C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27670C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5609C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5609C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5609C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5609C>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5609C>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 23445
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13550
  bin: 1.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

21-39823153-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823153
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823153
    reference: chr 21
allele count: 3
allele frequency: 5.127153404429861e-5
allele num: 58512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27670C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5609C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5609C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5609C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5609C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5609C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27670C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5609C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5609C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5609C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5609C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5609C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5609C>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13550
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23445
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

21-39823160-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823160
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823160
    reference: chr 21
allele count: 2
allele frequency: 3.420674557022645e-5
allele num: 58468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5616C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5616C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5616C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5616C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5616C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5616C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27677C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5616C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5616C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27677C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5616C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5616C>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5616C>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14122
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

21-39823169-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39823169
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39823169
    reference: chr 21
allele count: 1
allele frequency: 1.741007695254013e-5
allele num: 57438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-5625G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-40-27686G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.19-5625G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-5625G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.19-5625G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-5625G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.19-5625G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-5625G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-5625G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-27686G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.190-5625G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.19-5625G>A
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-5625G>A
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum

21-39870241-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39870241
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 39870241
    reference: chr 21
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000288319
  ensembl transcript: ENST00000288319
  gene symbol: ERG
  hgvsc: ENST00000288319.7:c.18+46A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000414150
  ensembl transcript: ENST00000417133
  gene symbol: ERG
  hgvsc: ENST00000417133.2:c.40-52697A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000396268
  ensembl transcript: ENST00000453032
  gene symbol: ERG
  hgvsc: ENST00000453032.2:c.-41+46A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000481609
  gene symbol: ERG
  hgvsc: ENST00000481609.1:n.94+46A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381879
  ensembl transcript: ENST00000398907
  gene symbol: ERG
  hgvsc: ENST00000398907.1:c.18+46A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381871
  ensembl transcript: ENST00000398897
  gene symbol: ERG
  hgvsc: ENST00000398897.1:c.-40-74758A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000415659
  ensembl transcript: ENST00000429727
  gene symbol: ERG
  hgvsc: ENST00000429727.2:c.18+46A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381891
  ensembl transcript: ENST00000398919
  gene symbol: ERG
  hgvsc: ENST00000398919.2:c.40-52697A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000485493
  gene symbol: ERG
  hgvsc: ENST00000485493.1:n.226-24197A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381882
  ensembl transcript: ENST00000398911
  gene symbol: ERG
  hgvsc: ENST00000398911.1:c.40-52697A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381881
  ensembl transcript: ENST00000398910
  gene symbol: ERG
  hgvsc: ENST00000398910.1:c.40-52697A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000381877
  ensembl transcript: ENST00000398905
  gene symbol: ERG
  hgvsc: ENST00000398905.1:c.18+46A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl protein: ENSP00000394694
  ensembl transcript: ENST00000442448
  gene symbol: ERG
  hgvsc: ENST00000442448.1:c.40-52697A>T
  variant of: http://identifiers.org/hgnc/3446
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157554
  ensembl transcript: ENST00000468474
  gene symbol: ERG
  hgvsc: ENST00000468474.1:n.226-52697A>T
  variant of: http://identifiers.org/hgnc/3446
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5436
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6603
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: DP

GenotypeDepth
all individuals: 340
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 124
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 101
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 76
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 496
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2788
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2141
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1018
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50746
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4328
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49842555105713e-5
allele num: 66690
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: 8648
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.307e1

FS
type: SiteQuality
SIO_000300: 1.149e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.558e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.44e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

DP
type: SiteQuality
SIO_000300: 1.520189e6

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

GenotypeDepth
all individuals: 100
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 234
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2793
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2139
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1020
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50809
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4319
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.520364e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

QD
type: SiteQuality
SIO_000300: 1.259e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.978e1

MQRankSum
type: SiteQuality
SIO_000300: -2.49e-1

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

GenotypeDepth
all individuals: 13439
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 97
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 816
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4305
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 989
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.594258042199931e-4
allele num: 11564
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998770504093322e-5
allele num: 66694
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.72e-1

DP
type: SiteQuality
SIO_000300: 1.520725e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

QD
type: SiteQuality
SIO_000300: 1.129e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 91
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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ReadPosRankSum
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InbreedingCoeff
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MQ
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DP
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MQRankSum
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QD
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FS
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VQSLOD
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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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allele frequency: 0.0e0
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South Asian
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East Asian
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Latino
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African
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European (Non-Finnish)
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Other
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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South Asian
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African
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European (Finnish)
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VQSLOD
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QD
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MQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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FS
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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Latino
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East Asian
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Other
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European (Finnish)
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QD
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DP
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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FS
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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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GenotypeQuality
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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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Other
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ClippingRankSum
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BaseQRankSum
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DP
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FS
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VQSLOD
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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East Asian
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Latino
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South Asian
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European (Finnish)
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Other
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QD
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ClippingRankSum
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VQSLOD
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FS
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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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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East Asian
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Latino
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African
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Other
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European (Non-Finnish)
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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MQ
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VQSLOD
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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Other
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African
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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QD
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ClippingRankSum
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DP
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Finnish)
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Other
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African
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QD
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FS
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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VQSLOD
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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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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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European (Finnish)
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African
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South Asian
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Latino
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QD
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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MQ
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DP
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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European (Finnish)
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East Asian
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African
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ReadPosRankSum
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VQSLOD
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MQ
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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QD
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DP
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GenotypeDepth
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Latino
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African
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East Asian
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South Asian
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VQSLOD
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QD
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MQ
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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MQRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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East Asian
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
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MQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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InbreedingCoeff
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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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European (Finnish)
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East Asian
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African
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South Asian
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Other
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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MQ
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ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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FS
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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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African
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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ClippingRankSum
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QD
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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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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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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African
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Other
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MQ
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VQSLOD
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DP
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MQRankSum
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InbreedingCoeff
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QD
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FS
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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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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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European (Non-Finnish)
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Latino
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South Asian
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African
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European (Finnish)
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East Asian
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FS
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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African
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East Asian
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European (Finnish)
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Latino
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Other
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MQRankSum
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BaseQRankSum
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QD
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VQSLOD
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DP
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQ
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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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GenotypeQuality
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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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South Asian
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East Asian
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European (Non-Finnish)
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African
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Other
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Latino
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QD
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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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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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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East Asian
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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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ReadPosRankSum
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VQSLOD
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QD
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FS
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BaseQRankSum
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MQ
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ClippingRankSum
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MQRankSum
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DP
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InbreedingCoeff
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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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allele count: 0
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Latino
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South Asian
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European (Finnish)
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Other
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East Asian
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European (Non-Finnish)
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QD
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ClippingRankSum
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InbreedingCoeff
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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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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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South Asian
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East Asian
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African
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Other
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QD
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InbreedingCoeff
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ReadPosRankSum
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FS
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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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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Latino
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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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African
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European (Finnish)
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FS
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MQRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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MQ
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VQSLOD
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ClippingRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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European (Non-Finnish)
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East Asian
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DP
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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QD
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FS
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MQRankSum
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VQSLOD
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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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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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South Asian
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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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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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MQ
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FS
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QD
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MQRankSum
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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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South Asian
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African
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Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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European (Non-Finnish)
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ClippingRankSum
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DP
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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QD
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MQ
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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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Other
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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InbreedingCoeff
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ReadPosRankSum
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DP
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FS
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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QD
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VQSLOD
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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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South Asian
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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East Asian
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VQSLOD
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DP
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQ
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QD
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MQRankSum
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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Latino
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East Asian
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African
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South Asian
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MQ
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MQRankSum
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QD
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VQSLOD
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FS
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ReadPosRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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African
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BaseQRankSum
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MQ
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FS
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QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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VQSLOD
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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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South Asian
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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FS
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ReadPosRankSum
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QD
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BaseQRankSum
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MQ
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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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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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Other
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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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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InbreedingCoeff
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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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South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 3.781194857574994e-4
allele num: 7934
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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Latino
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Other
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QD
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ReadPosRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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FS
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VQSLOD
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MQ
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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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GenotypeQuality
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GenotypeQuality
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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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African
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allele num: 9706
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Latino
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Other
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DP
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FS
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MQRankSum
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QD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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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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African
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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Latino
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East Asian
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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DP
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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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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European (Finnish)
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European (Non-Finnish)
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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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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1646
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4552
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.340842048806651e-4
allele num: 7458
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
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ClippingRankSum
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SIO_000300: -1.699e0

DP
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SIO_000300: 2.3455e5

FS
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SIO_000300: 5.76e0

InbreedingCoeff
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SIO_000300: -1.86e-2

VQSLOD
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SIO_000300: -1.6e-2

ReadPosRankSum
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SIO_000300: 1.47e0

MQRankSum
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SIO_000300: -6.04e-1

MQ
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SIO_000300: 5.942e1

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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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4713
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.332622601279318e-4
allele num: 7504
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1662
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4762
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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BaseQRankSum
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SIO_000300: -3.307e0

ReadPosRankSum
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SIO_000300: 4.42e-1

QD
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SIO_000300: 1.031e1

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -2.16e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 2.38985e5

ClippingRankSum
type: SiteQuality
SIO_000300: -8.38e-1

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: 629
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4966
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.339046598821639e-4
allele num: 7468
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1694
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.27e-1

FS
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SIO_000300: 7.385e0

InbreedingCoeff
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SIO_000300: -2.91e-2

MQRankSum
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ClippingRankSum
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SIO_000300: 4.61e-1

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -9.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 8.68e0

DP
type: SiteQuality
SIO_000300: 2.40852e5

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3409
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variant carriers: 0

GenotypeQuality
all individuals: 1752
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4674
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3372
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3772
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.33153e2

MQRankSum
type: SiteQuality
SIO_000300: -3.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e0

DP
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SIO_000300: 7.55311e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.784e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

MQ
type: SiteQuality
SIO_000300: 5.729e1

QD
type: SiteQuality
SIO_000300: 2.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.55e-1

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 31

GenotypeDepth
all individuals: 1834
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variant carriers: 79

GenotypeQuality
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variant carriers: 46

GenotypeQuality
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variant carriers: 12

GenotypeQuality
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variant carriers: 77

GenotypeQuality
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variant carriers: 48

GenotypeQuality
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variant carriers: 74

GenotypeQuality
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variant carriers: 60

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 88

GenotypeQuality
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GenotypeQuality
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variant carriers: 65

GenotypeQuality
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variant carriers: 76

GenotypeQuality
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GenotypeQuality
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variant carriers: 77

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 248

GenotypeQuality
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variant carriers: 66

GenotypeQuality
all individuals: 249
bin: 8.75e1
variant carriers: 31

GenotypeQuality
all individuals: 445
bin: 8.25e1
variant carriers: 38

European (Non-Finnish)
type: Population
allele count: 456
allele frequency: 2.571041948579161e-2
allele num: 17736
num of homozygotes: 0

Latino
type: Population
allele count: 62
allele frequency: 3.575547866205306e-2
allele num: 1734
num of homozygotes: 0

African
type: Population
allele count: 90
allele frequency: 5.325443786982249e-2
allele num: 1690
num of homozygotes: 0

Other
type: Population
allele count: 13
allele frequency: 4.609929078014184e-2
allele num: 282
num of homozygotes: 0

East Asian
type: Population
allele count: 79
allele frequency: 5.019059720457433e-2
allele num: 1574
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 2.329002206423143e-3
allele num: 8158
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 266
allele frequency: 1.551925320886814e-1
allele num: 1714
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.30953e2

InbreedingCoeff
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SIO_000300: -8.690000000000001e-2

DP
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SIO_000300: 6.78101e5

BaseQRankSum
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SIO_000300: -2.426e0

ClippingRankSum
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SIO_000300: -3.87e-1

QD
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SIO_000300: 2.32e0

MQRankSum
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SIO_000300: 1.13e-1

ReadPosRankSum
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SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.409999999999999e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.624238909828936e-5
allele num: 27592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3736
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3380
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VQSLOD
type: SiteQuality
SIO_000300: -1.016e2

MQ
type: SiteQuality
SIO_000300: 5.717e1

FS
type: SiteQuality
SIO_000300: 1.47291e2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

ReadPosRankSum
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SIO_000300: -1.338e0

InbreedingCoeff
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SIO_000300: -8.800000000000001e-3

DP
type: SiteQuality
SIO_000300: 7.02598e5

QD
type: SiteQuality
SIO_000300: 2.71e0

BaseQRankSum
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SIO_000300: -3.0e0

GenotypeDepth
all individuals: 46
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variant carriers: 0

GenotypeDepth
all individuals: 190
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GenotypeDepth
all individuals: 47
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 364
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GenotypeQuality
all individuals: 606
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2982
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3210
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.150518412584913e-5
allele num: 27970
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.04239e5

MQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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SIO_000300: -9.900000000000001e-3

BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 3.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.139e1

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 526
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4330
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2924
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4525
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2595
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5516
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1227
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20961
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3109
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4128
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2962
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9428
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.93e-1

FS
type: SiteQuality
SIO_000300: 9.708e1

VQSLOD
type: SiteQuality
SIO_000300: -4.681e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.619e0

QD
type: SiteQuality
SIO_000300: 3.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.833e0

MQ
type: SiteQuality
SIO_000300: 5.662e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.32e-1

DP
type: SiteQuality
SIO_000300: 7.06357e5

GenotypeDepth
all individuals: 46
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 137
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4305
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3313
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3499
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1461
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 399
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2962
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28050
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9436
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.813e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.04e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

QD
type: SiteQuality
SIO_000300: 5.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.1053e5

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 4187
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21824
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1237
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 881
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2500
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5412
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 414
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 616
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 357
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4365
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 673
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3353
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2872
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 4.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 9
allele frequency: 3.088538091969801e-3
allele num: 2914
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.917152858809801e-4
allele num: 3428
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.538071065989848e-3
allele num: 394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.176175098672408e-5
allele num: 27870
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.148614609571788e-4
allele num: 3176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9398
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.922e0

MQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

DP
type: SiteQuality
SIO_000300: 7.12394e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.938e0

FS
type: SiteQuality
SIO_000300: 1.43296e2

MQ
type: SiteQuality
SIO_000300: 5.892e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.16e-2

QD
type: SiteQuality
SIO_000300: 6.02e0

VQSLOD
type: SiteQuality
SIO_000300: -9.397e1

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23754
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5257
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
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variant carriers: 0

GenotypeQuality
all individuals: 4204
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
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variant carriers: 0

GenotypeQuality
all individuals: 4384
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2433
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2452
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4037
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2459
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1286
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.537068477645727e-5
allele num: 28272
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3002
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3808
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.99e0

QD
type: SiteQuality
SIO_000300: 8.220000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.01e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.847e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.072e0

DP
type: SiteQuality
SIO_000300: 7.20281e5

MQRankSum
type: SiteQuality
SIO_000300: -1.036e0

GenotypeDepth
all individuals: 1779
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
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variant carriers: 0

GenotypeDepth
all individuals: 532
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 632
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variant carriers: 0

GenotypeQuality
all individuals: 26190
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4171
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1862
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3960
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1395
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
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variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5957
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1352
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3908
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1492
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3944
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28978
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 2.927400468384075e-4
allele num: 3416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3618
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.107e0

FS
type: SiteQuality
SIO_000300: 2.963e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

DP
type: SiteQuality
SIO_000300: 7.52503e5

MQRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

QD
type: SiteQuality
SIO_000300: 4.72e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

GenotypeDepth
all individuals: 535
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27207
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
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GenotypeQuality
all individuals: 1494
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variant carriers: 1

GenotypeQuality
all individuals: 3582
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3684
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7456
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3603
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1340
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
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GenotypeQuality
all individuals: 335
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
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GenotypeQuality
all individuals: 394
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
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GenotypeQuality
all individuals: 349
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GenotypeQuality
all individuals: 726
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GenotypeQuality
all individuals: 1042
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GenotypeQuality
all individuals: 1383
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3724
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.738e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

DP
type: SiteQuality
SIO_000300: 7.7312e5

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.638e0

QD
type: SiteQuality
SIO_000300: 4.64e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 533
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variant carriers: 0

GenotypeQuality
all individuals: 892
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variant carriers: 0

GenotypeQuality
all individuals: 273
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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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variant carriers: 0

GenotypeQuality
all individuals: 3352
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8211
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variant carriers: 0

GenotypeQuality
all individuals: 1495
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1121
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.75e1
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GenotypeQuality
all individuals: 362
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
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GenotypeQuality
all individuals: 865
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 723
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variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3254
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.42600679281902e-4
allele num: 4122
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9624
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.514e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.82314e5

QD
type: SiteQuality
SIO_000300: 5.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

GenotypeDepth
all individuals: 138
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variant carriers: 0

GenotypeDepth
all individuals: 33
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variant carriers: 0

GenotypeDepth
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 8933
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variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 353
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4174
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.624671916010499e-4
allele num: 3810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 9.935748824269723e-5
allele num: 30194
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

FS
type: SiteQuality
SIO_000300: 8.233000000000001e0

QD
type: SiteQuality
SIO_000300: 1.18e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

DP
type: SiteQuality
SIO_000300: 7.91525e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

GenotypeDepth
all individuals: 72
bin: 7.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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: 1

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3418
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.554931016862545e-4
allele num: 3914
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3692
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.416e0

MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 4.065e0

DP
type: SiteQuality
SIO_000300: 8.07671e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-2

QD
type: SiteQuality
SIO_000300: 1.368e1

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 246
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variant carriers: 0

GenotypeDepth
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 472
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variant carriers: 0

GenotypeQuality
all individuals: 27616
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
all individuals: 588
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 731
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 371
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GenotypeQuality
all individuals: 1122
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3740
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.116073266104137e-4
allele num: 9718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30996
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.708e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

VQSLOD
type: SiteQuality
SIO_000300: 4.79e-1

QD
type: SiteQuality
SIO_000300: 1.008e1

DP
type: SiteQuality
SIO_000300: 8.12818e5

GenotypeDepth
all individuals: 118
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
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variant carriers: 0

GenotypeDepth
all individuals: 1056
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variant carriers: 0

GenotypeQuality
all individuals: 11788
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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
all individuals: 1502
bin: 9.75e1
variant carriers: 4

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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2590
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 884
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variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4650
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3972
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.234339319879035e-4
allele num: 32406
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.40512e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.599999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12683
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variant carriers: 1

GenotypeDepth
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 1338
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variant carriers: 0

GenotypeQuality
all individuals: 273
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GenotypeQuality
all individuals: 505
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GenotypeQuality
all individuals: 8172
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GenotypeQuality
all individuals: 729
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GenotypeQuality
all individuals: 649
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 306
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variant carriers: 0

GenotypeQuality
all individuals: 3483
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GenotypeQuality
all individuals: 309
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variant carriers: 0

GenotypeQuality
all individuals: 3052
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variant carriers: 0

GenotypeQuality
all individuals: 867
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variant carriers: 0

GenotypeQuality
all individuals: 799
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variant carriers: 0

GenotypeQuality
all individuals: 1499
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variant carriers: 1

GenotypeQuality
all individuals: 28199
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variant carriers: 0

GenotypeQuality
all individuals: 3287
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variant carriers: 0

GenotypeQuality
all individuals: 367
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variant carriers: 0

GenotypeQuality
all individuals: 1155
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variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.101929400086854e-5
allele num: 32238
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

FS
type: SiteQuality
SIO_000300: 2.398e0

VQSLOD
type: SiteQuality
SIO_000300: -2.329e0

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

ReadPosRankSum
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SIO_000300: 1.25e0

BaseQRankSum
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.0414e5

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

GenotypeDepth
all individuals: 2775
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2551
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variant carriers: 1

GenotypeDepth
all individuals: 138
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GenotypeQuality
all individuals: 334
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1306
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GenotypeQuality
all individuals: 372
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4128
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.552322613578356e-4
allele num: 3918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3762
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32060
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.92743e5

MQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

QD
type: SiteQuality
SIO_000300: 5.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.5e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

GenotypeDepth
all individuals: 1837
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variant carriers: 0

GenotypeDepth
all individuals: 73
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variant carriers: 1

GenotypeDepth
all individuals: 51
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GenotypeQuality
all individuals: 390
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 864
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 1571
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variant carriers: 71

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 648
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GenotypeQuality
all individuals: 500
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GenotypeQuality
all individuals: 6562
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GenotypeQuality
all individuals: 376
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variant carriers: 7

GenotypeQuality
all individuals: 723
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GenotypeQuality
all individuals: 399
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variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 8.718395815170009e-4
allele num: 4588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 49
allele frequency: 1.533262406909068e-3
allele num: 31958
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.951921101294432e-3
allele num: 9734
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 4.844961240310077e-4
allele num: 4128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 5.341880341880342e-4
allele num: 3744
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.183406113537118e-3
allele num: 458
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

DP
type: SiteQuality
SIO_000300: 7.88703e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1054
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1834
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3435
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 864
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31958
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.081980686254366e-4
allele num: 9734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4588
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

FS
type: SiteQuality
SIO_000300: 5.35e-1

DP
type: SiteQuality
SIO_000300: 7.88703e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

QD
type: SiteQuality
SIO_000300: 1.225e1

GenotypeDepth
all individuals: 192
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3634
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3709
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.26527159952384e-5
allele num: 31922
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3754
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.16e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.553e0

QD
type: SiteQuality
SIO_000300: 3.45e0

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.49e-1

FS
type: SiteQuality
SIO_000300: 5.164e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.21e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

DP
type: SiteQuality
SIO_000300: 7.77882e5

GenotypeDepth
all individuals: 50
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25910
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1827
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1932
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1949
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 364
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4130
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4807
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5456
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3706
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 643
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1299
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3712
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4082
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31312
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.0315659170621e-4
allele num: 9694
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.633e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.161e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.37e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.94e-1

FS
type: SiteQuality
SIO_000300: 1.6993e1

QD
type: SiteQuality
SIO_000300: 2.608e1

DP
type: SiteQuality
SIO_000300: 7.58015e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

GenotypeDepth
all individuals: 1416
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 7051
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6897
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1639
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 943
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 1453
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2002
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variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2679
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 81
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44330
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2190
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2826
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variant carriers: 0

GenotypeQuality
all individuals: 2511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.404103e6